American Medicals
United Statesfrom the FDA registration address FDA establishment FEI 3004552850
American Medicals is a medical device manufacturer, with 1,676 devices listed in FDA GUDID (FDA Class I) as of 12 Nov 2026.
- Devices
- 1,676
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 1,676
- Device classes
- FDA Class I 1,676
- Identifiers
- FDA FEI 3004552850
What American Medicals makes
American Medicals manufactures reusable surgical instruments, including coronary artery clamps, soft-tissue manipulation forceps (both scissors-like and tweezers-like), general-purpose surgical scissors, suturing needle holders, and self-retaining retractors. The company also produces single-use podiatric burs and reusable bone curettes, designed for precision in orthopedic and podiatric procedures.
All listed devices fall under Class I regulatory classification in the U.S. and are recorded in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 1,676 devicesShowing 1-50 of 1,676
Company details
- FDA FEI number
- 3004552850
- Address
- 8900 Corporate Square Ct, Jacksonville, FL, 32216
Frequently asked questions
How many devices does AMERICAN MEDICALS have in the registry?
The registry currently lists 1676 devices for AMERICAN MEDICALS. Devices recorded under merged duplicate company entries are counted once.
Which registries list AMERICAN MEDICALS's devices?
Among its 50 most recently registered devices, AMERICAN MEDICALS has devices listed in FDA GUDID (50 devices).
What risk classes do AMERICAN MEDICALS's devices fall under?
Among its 50 most recently registered devices, the classes recorded for AMERICAN MEDICALS's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from AMERICAN MEDICALS in the registry?
The most recently registered devices listed for AMERICAN MEDICALS include steriSTAT 1, American Medicals 1 and American Medical 1.