Bahadir USA LLC
United Statesfrom the FDA registration address FDA establishment FEI 3005741909
Bahadir USA LLC is a medical device manufacturer, with 870 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 870
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 866
- FDA 510(k) 4
- Device classes
- FDA Class II 570
- FDA Class I 300
- Identifiers
- FDA FEI 3005741909
What Bahadir USA LLC makes
The company produces reusable sterilization and disinfection containers, instrument trays designed for medical equipment, and single-use sterilization container filters. These products are intended for use in healthcare settings to hold, protect, and sterilize surgical instruments and devices.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 870 devicesShowing 1-50 of 870
Company details
- FDA FEI number
- 3005741909
- Address
- 431 S Pennsville Auburn Rd, Carneys Point, NJ, 08069
Frequently asked questions
How many devices does BAHADIR USA LLC have in the registry?
The registry currently lists 870 devices for BAHADIR USA LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list BAHADIR USA LLC's devices?
Among its 50 most recently registered devices, BAHADIR USA LLC has devices listed in FDA GUDID (50 devices).
What risk classes do BAHADIR USA LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for BAHADIR USA LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BAHADIR USA LLC in the registry?
The most recently registered devices listed for BAHADIR USA LLC include BAHADIR USA Y100.97M, BAHADIR USA Y105.92M, BAHADIR USA Y106.92M and BAHADIR USA Y110.92M.