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Key West, Monroe County, Florida
Asking Price
$250,000
Revenue
$11,000
Down
Call/Email
Cash Flow
$97,000
Posting ID:
284077
Business Category:
Restaurants & Food, Service, Entertainment
Business Types:
Event, Party & Wedding Service
Food Service
Keywords:
food festival
wine
event
key west
monroe
florida
Attributes:
Broker Cooperation
Financial Assistance
Owner/Seller Financing
Training And Support
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Seize a unique opportunity to acquire an established and reputable deep-sea fishing charter business in Key West, Florida, a globally renowned sportfishing destination. This is an exceptional chance to immerse yourself in the sought-after boating and fishing lifestyle, inheriting a fully operational enterprise poised for continued success. The sale includes a fully outfitted 47’ 1971 AMF Concord sportfishing vessel, professionally equipped for offshore charters, and a long-term lease of the most disputed marine slip in town. The business boasts significant name recognition, a loyal repeat clientele, a robust online presence, and established relationships with highly experienced local captains and mates. Notably, the current owner-operator is retiring. This opportunity is particularly compelling for licensed captains aspiring to independent ownership. A suitable transition period will be provided to ensure a seamless handover to the new owner. This authentic Key West charter business possesses a rich history and strong local recognition. It represents an ideal investment for a discerning buyer looking to harmonize a rewarding livelihood with the distinctive Key West lifestyle, celebrated worldwide for its pristine waters, breathtaking sunsets, and deep-rooted fishing traditions. Prospective buyers are required to submit a Non-Disclosure Agreement (NDA) and proof of funds to access detailed financial information and additional specifics. https://tworld.com/locations/Florida/fortlauderdale/listings/Famous-Key-West-Fishing-Charter-Business-for-Sale-

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Los Angeles, California
Gene And Cell Therapy Regulatory Consulting
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Founded in 2011, the Company is a niche consulting and advisory firm serving in cell therapy, gene and gene-modified cell therapies, other regenerative medicines, tissue engineering, and cell-based drug discovery. The company's core focus is to improve cell & gene therapy innovations by providing consulting services for improving business strategy and achieving major regulatory milestones for companies. The Company has created a one-stop shop for all aspects of cell therapy and gene therapy, including quality checks, regulatory meetings, and submissions with the help of leading experts worldwide. The leadership has a unique combination of experience in the academic, biotech industry, government/FDA, and consulting. They serve biotech, pharma companies, consulting services for healthcare providers, subcontracts for other consulting firms, and contracts with government organizations, which enables them to have 6x+ growth in net income from 2019 2021, i.e., $179,000 to $1,095,000 with the help of 110+ customers served over the past six years. The Company's plan is to consummate a transaction with a supportive growth partner in order to accelerate the company's cell and gene therapy market growth by interacting with industry, academia, government, and other international stakeholders in cell & gene therapies and cell-based drug discovery. NDA is required to secure comprehensive Confidential Information Memorandum (CIM) crafted by ProNova Partners. Detailed Information Facilities: Has headquarters in US contractors operate nationwide / portable / buyer can be located worldwide. Competition: A few competitors in the space are in the field but the Company provides best in class services for its respective niche(s). Growth & Expansion: Continually grow and become more profitable with the help of experts that supports preclinical, clinical, and commercial advisory in the manufacturing, regulatory affairs, Quality/GxP, and M&A arenas. Financing: If the price and deal structure is right. Support & Training: Long term transition, Seller wishes to smooth the transition to maximize success with the Company post-closing and spearhead continued growth. Reason for Selling: Growth.

Hillsborough, New Jersey
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Our client is offering a next generation, patented medical device for the treatment of internal hemorrhoids. The procedure is painless, non-invasive, requires no anesthesia, is conducted in under 2 minutes, and can be performed in any medical setting: a doctor's office, a surgery center, an endo suite, or a hospital. Our client's product is a small, disposable, medical device that eliminates hemorrhoids. A physician uses this device by deploying a tiny rubber band on the base of the hemorrhoid. This procedure is known as rubber band ligation, and it is the #1 recommended treatment for internal hemorrhoids by the American College of Gastroenterology. Patients no longer need to use ineffective creams or receive painful, invasive surgery. Our client's device offers a permanent solution for their hemorrhoids. The device is currently manufactured in the USA through an FDA approved, ISO 13485 contract manufacturer, who specializes in medical devices. The device is sold directly to physicians of different specialties, including gastroenterologists, colorectal surgeons, GYNs, urologists and primary care physicians. The biggest targeted audience are gastroenterologists. NDA is required to secure comprehensive Confidential Information Memorandum. Growth and epansion: Nearly half of adults over the age of 50 will develop symptomatic hemorrhoids. In the U.S. alone, an estimated 60,000,000 people have experienced hemorrhoid symptom(s) at some point in their lives. Annually, over 20,000,000 people in the U.S. use an over-the-counter hemorrhoid treatment and 75% report a reoccurrence. These patients no longer need to use ineffective creams or receive painful, invasive surgery. Our client's device offers a permanent solution for their hemorrhoids. Financing is if the price and deal structure is right, and support and training is provided as required. Facilities are Outlined in CIM. Reason for selling is that the owners wish to move on to other projects.

Milwaukee, Wisconsin
Therapeutic Rehab Tech Platform Recurring Revenue
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The company is a developer of an advanced therapeutic technology platform specializing in neuromuscular stimulation solutions designed to restore strength and function for patients with limited mobility. The internationally patented, FDA-registered product leverages space medicine technology invented by the company founder to serve as a countermeasure to disuse atrophy during long duration spaceflight. The company adapted this technology for use by frail older adults using funds from a National Institute on Aging (NIA) Small Business Innovation Research (SBIR) grant. The company has since evolved the internationally patented technology to enable controlled, patient specific neuromuscular stimulation that activates muscles passively and has been shown in multiple studies to significantly reduce pain and improve sensation / reduce neuropathy symptoms. To better deliver the neuromuscular stimulation, the company has incorporated AI-driven robotics to provide engaging, interactive workouts that patients enjoy. This advanced technology-based platform has been designed to collect treatment data that will be used for predictive analytics and to create AI-based user instructions that adapt treatment protocols in real-time to arrive at optimal patient outcomes. It provides safe, progressive treatments to the most vulnerable patients while unlocking new revenue streams and cost savings for customers. The platform has demonstrated strong clinical outcomes in over 2 dozen studies backed by NIH-funded research and pilot programs in hospitals, therapy gyms, skilled nursing, and senior living facilities. The value proposition for customers is strong (value of healthcare = outcomes x patient satisfaction x revenue / costs) because of the incredible outcomes and satisfaction achieved combined with treatments for lower functioning individuals being reimbursable by Medicare and insurance while also providing significant cost savings on the costliest population. Operating on a capital-efficient, scalable model, the company employs commission-based sales and contract manufacturing to maintain lean overhead while enabling rapid expansion. With a growing clinical customer pipeline, a transition to recurring revenue through subscription and leasing models, and an increase in expected gross margins from 68% in year 1 to 90% in year 2, the business is positioned to scale within the $250B+ global medtech market. It is actively expanding into home health and veteran care channels and pursuing strategic partnerships to broaden its commercial footprint. NDA is required to secure the comprehensive Confidential Information Memorandum (CIM) crafted by ProNova Partners.

Irvine, California
Pharmaceutical Company - Targeting Drug Delivery
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Patented Universal Tumor-Targeting Drug Delivery Platform Co. This pharmaceutical company has developed and patented a universal tumor-targeting drug-delivery platform that can improve the safety and efficacy of many existing chemo treatments, with the ability to target numerous different types of cancer. The technology encapsulates existing FDA-approved drugs inside lipid nanoparticles (liposomes or emulsions) coated with patented human-sourced antinuclear antibodies (ANA). The lipid nanoparticle provides long-term storage stability of the drug and controlled release of the drug over time at body-temperature, and is expected to improve the safety and efficacy profile of the drug, including passive accumulation at the tumor while not harming normal tissues. The Company's ANA, sourced from lupus patients, binds to nuclear material present in abundance in areas of necrosis (dead / ruptured cells) present in and around all solid tumors, thus anchoring the drug-filled nanoparticles at the tumor where the nanoparticle is designed to slowly release the drug directly on the tumor for more effect. As the Company's ANA is not tumor-marker specific, but rather targets necrosis present in solid tumors, the technology is designed to "universally" target many different types of cancer including breast cancer, lung, ovarian, colon, prostate, etc., as well as rare childhood cancers. The Company completed a successful proof-of-concept study at Children's Hospital using Ewing's Sarcoma transplanted in immunodeficient mice. Treatment with the Company's forumlation significantly inhibited tumor growth and extended survival times compared to control mice receiving no treatment or treatment with plain liposomal doxorubicin. The Company has been granted Orphan Drug Designation by the FDA on 2 of the lead drug formulations, providing FDA fee waivers, priority review, and 7-years exclusivity upon market approval. The orphan pathway also enables the potential for New Drug Approval after successful completion of Phase 2 studies, with Phase III data collected while in the market, thus significantly lowering the time and cost to market approval. This same drug inside the Company's tumor targeting delivery system will likely have potential to treat other pediatric cancers, and/or cancers in larger adult populations. As the Company's platform and ANA has the potential to improve the safety and efficacy of many existing FDA approved drugs or even compounds in development, the Company anticipates the potential for multiple licensing agreements with multiple pharmaceutical companies seeking to improve their existing portfolio and extend patient life as they advance into clinical stage. And as it may be possible to file for New Drug Approval following successful Phase II studies, the Company anticipates licensing potential at early clinical stage. Multiple exit opportunities exist with high impact & high ROI. The Company is seeking a supportive capital partner to maintain momentum up to $20M. Funding will be used to advance the lead drug through formal Investigational New Drug enabling studies towards New Drug Approval; estimating $3-5 Million now to advance into clinical studies. Preclinical / animal studies estimate ($3 - 5 Million and 12-18 months); follwed by potential combined Phase I-II clinical study in a rare cancer (approximately 2-3 years and $10M) to potential New Drug Approval, plus additional capital to advance additional drugs in the pipeline simultaneously, thus adding tremendous value to the Company's valuation. Valuations of pharma companies often exceed $100 Million valuation at Phase I (approx. 18 months), and New Drug Approval can exceed valuations above $1 Billion. The Company has numerous, improved high-impact cancer drugs advancing with proper support. NDA is required for comprehensive Confidential Information Memorandum crafted by ProNova Partners. Detailed Information Competition: Trying to improve existing therapies and develop novel approaches to hard to treat cancers. Growth & Expansion: Huge market potential. Financing: If the price and deal structure is right. Support & Training: Transition team included. Reason for Selling: Seeking supportive capital partners to take to the next level(s). .

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Storied Civil & Structural Engineering Firm for Sale
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CF : $ 170,334
A leading regional civil and structural engineering firm specializing in residential, commercial, and municipal projects. Core expertise includes slope stability, erosion control, and landslide remediation, along with structural design for churches, office buildings, and bridge reconstructions. Collaborating with specialized sub-consultants in geotechnical, hydraulic, and architectural disciplines, the firm delivers innovative gabion and soldier-pile solutions that enhance safety, cost efficiency, and sustainability while maintaining long-term client relationships. The owner is seeking to transition into retirement after a long and successful career in engineering, with plans to focus on writing and publishing in the coming years. NDA is required to receive comprehensive Confidential Information Memorandum (CIM) crafted by ProNova Partners.

Lafayette, Louisiana
Artisanal Master Charcutier: Dominant Market Position
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CF : $ 151,600
This classically trained chef interned in Napa Valley before returning to Georgia with a big idea for this business. With his wife as co-owner, they began producing small-batch salami from a 200-square-foot shared kitchen and attending weekly farmers’ markets. With 2025 revenue nearly reaching $4M, and numerous annual awards for innovative and flavorful meats, the operation continues to focus on small-batch charcuterie, blending traditional European methods with distinct regional ingredients to create meat products of unparalleled quality. Items are sliced and packaged in-house or shipped to a regional co-packer. The company operates across five primary revenue channels: retail sales, national distribution, farmers' markets, direct business-to-business sales, and co-packing and white-labeling. Additional growth opportunities exist in direct-to-consumer online fulfillment. The initial placement at grocery stores has already been completed, with the addition of a new commercial client booked in January 2026. The next step is achieving a larger footprint with big-box and secured retailers. An NDA is required to receive a comprehensive Confidential Information Memorandum (CIM) crafted by ProNova Partners. Detailed Information: Facilities: The Company’s headquarters features more than 7,000 square feet of retail, office, production, and cold storage space. The Company owns the building, located at a busy city intersection, and pays through $18,500. The last property appraisal for the real estate was at $2.8M. Competition: The Company competes in a crowded market dominated by large international brands that focus on commodity meats and traditional flavors. Its competitive advantage lies in humanely sourced proteins and a differentiated, artisanal approach, supported by award-winning products and a distinctive, trademarked brand identity. Growth & Expansion: With proven demand, a scalable model, and a fully designed expansion plan ready for execution, additional expansion into local, regional, national, and international footprints would be significant. Additionally, streamlining SKUs to focus on products with the highest margins, bringing slicing and packaging in-house, or integrating automation will unlock production efficiencies. Expansion into international markets would also be an additional path to growth. Financing: If deal terms and structure are acceptable. Support & Training: The company’s founder and creative lead would prefer to remain actively involved following the sale, depending on the transaction structure. His expertise in preserving the company’s distinct identity, flavor profiles, and market position would be valuable. While a complete exit is preferred for the second partner, both are committed to facilitating a seamless transfer of responsibilities. Reason for Selling: Keeping up with demand requires a strategic partner to efficiently scale the operations.
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