Marine Polymer Technologies, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3001237365
Marine Polymer Technologies, Inc. is a medical device manufacturer, with 27 devices listed in FDA GUDID and FDA 510(k) (FDA Class I, Unclassified and Class II) as of 13 Nov 2026.
- Devices
- 27
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 17
- FDA 510(k) 10
- Device classes
- FDA Class I 15
- FDA Unclassified 7
- FDA Class II 5
- Identifiers
- FDA FEI 3001237365
Catalogue
Search and filter all 27 devicesCompany details
- FDA FEI number
- 3001237365
- Address
- 461 BOSTON ST., UNIT B5, TOPSFIELD, MA, 01983
Frequently asked questions
How many devices does MARINE POLYMER TECHNOLOGIES, INC. have in the registry?
The registry currently lists 27 devices for MARINE POLYMER TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MARINE POLYMER TECHNOLOGIES, INC.'s devices?
Among its 27 most recently registered devices, MARINE POLYMER TECHNOLOGIES, INC. has devices listed in FDA 510(k) (10 devices) and FDA GUDID (17 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MARINE POLYMER TECHNOLOGIES, INC.'s devices fall under?
Among its 27 most recently registered devices, the classes recorded for MARINE POLYMER TECHNOLOGIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from MARINE POLYMER TECHNOLOGIES, INC. in the registry?
The most recently registered devices listed for MARINE POLYMER TECHNOLOGIES, INC. include Syvek Brace with Straps 420-05, Syvek Radial Patch 400-29, mrdh Bandage 5 cm x 5 cm 400-25 and SyvekExcel Vascular Access Hemostasis System 400-16-05.