Medicraft Inc
Also registered as Medi-Craft, Ltd.
United Statesfrom the FDA registration address FDA establishment FEI 3009538923
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Oxygen Connecting Tubes Ref K800504
Regimes: 510(k) Registry: 510(k)Stomach Tubes Ref K800508
Regimes: 510(k) Registry: 510(k)Urethral Catheter Ref K800505
Regimes: 510(k) Registry: 510(k)Suction Catheter Ref K800503
Regimes: 510(k) Registry: 510(k)Feeding Tubes Ref K800507
Regimes: 510(k) Registry: 510(k)Oxygen Catheter Ref K800506
Regimes: 510(k) Registry: 510(k)Rectal & Harris Flush Tubes Ref K800510
Regimes: 510(k) Registry: 510(k)Connecting Tubes Ref K800509
Regimes: 510(k) Registry: 510(k)Suction Catheter Kit Ref K861949
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009538923
- Address
- 50 Bushes Ln, Elmwood Park, NJ, 07407
Frequently asked questions
How many devices does Medicraft Inc have in the registry?
The registry currently lists 9 devices for Medicraft Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medicraft Inc's devices?
Among its 9 most recently registered devices, Medicraft Inc has devices listed in FDA 510(k) (9 devices).
What risk classes do Medicraft Inc's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Medicraft Inc's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medicraft Inc in the registry?
The most recently registered devices listed for Medicraft Inc include OXYGEN CONNECTING TUBES, STOMACH TUBES, URETHRAL CATHETER and SUCTION CATHETER.