Marina Medical Instruments, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000124817
Marina Medical Instruments, Inc. is a medical device manufacturer, with 3,696 devices listed and 3 FDA recalls as of 12 Nov 2026.
- Devices
- 3,696
- Registrations
- FDA
- FDA recalls
- 3
Registry facts
- Registries
- FDA GUDID 3,000
- Device classes
- FDA Class I 2,787
- FDA Class II 213
- FDA recalls
- Identifiers
- FDA FEI 1000124817
What Marina Medical Instruments, Inc. makes
Marina Medical Instruments, Inc. manufactures reusable surgical instruments, including vascular dilators, general-purpose surgical scissors, alligator-style soft-tissue forceps, reusable vaginal speculums, liposuction cannulas, suturing needle holders, and dressing forceps. The company also produces a vaginal dilator designed for medical procedures.
The company’s products are regulated under FDA’s 510(k) clearance process, with devices classified as Class I and Class II. These instruments are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations.
Catalogue
Search and filter all 3,696 devicesShowing 1-50 of 3,696
Company details
- FDA FEI number
- 1000124817
- Address
- 8190 West State Road 84, Davie, FL, 33324
FDA recalls
FDA recall records list 3 recalls initiated by MARINA MEDICAL INSTRUMENTS, INC., initiated on 2009-04-09. By recorded status: 3 terminated. The reasons filed fall into these groups: manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2009
- 9 Apr 2009 Z-1206-2010 Unclassified (pre-2012) Terminated Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation.
- 9 Apr 2009 Z-1207-2010 Unclassified (pre-2012) Terminated Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation.
- 9 Apr 2009 Z-1208-2010 Unclassified (pre-2012) Terminated Marina Medical, Sunrise, FL initiated recall of 46 products of 350 series devices and 47 products of 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation.
Frequently asked questions
How many devices does MARINA MEDICAL INSTRUMENTS, INC. have in the registry?
The registry currently lists 3696 devices for MARINA MEDICAL INSTRUMENTS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MARINA MEDICAL INSTRUMENTS, INC.'s devices?
Among its 50 most recently registered devices, MARINA MEDICAL INSTRUMENTS, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do MARINA MEDICAL INSTRUMENTS, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for MARINA MEDICAL INSTRUMENTS, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for MARINA MEDICAL INSTRUMENTS, INC.?
FDA recall records list 3 recalls initiated by MARINA MEDICAL INSTRUMENTS, INC., the most recent initiated on 9 Apr 2009. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from MARINA MEDICAL INSTRUMENTS, INC. in the registry?
The most recently registered devices listed for MARINA MEDICAL INSTRUMENTS, INC. include Marina Medical 800-524, Marina Medical 800-512, Marina Medical 08-0165 and Marina Medical 050-128SC.