Toetal Solutions, Inc
United Statesfrom the FDA registration address FDA establishment FEI 3026032087
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
ZipToe™ Hammertoe Fusion System Ref K253325
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3026032087
- Address
- 7 Great Valley Pkwy Ste 295, Malvern, PA, 19355
Frequently asked questions
How many devices does TOETAL SOLUTIONS, INC have in the registry?
The registry currently lists 6 devices for TOETAL SOLUTIONS, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list TOETAL SOLUTIONS, INC's devices?
Among its 6 most recently registered devices, TOETAL SOLUTIONS, INC has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do TOETAL SOLUTIONS, INC's devices fall under?
Among its 6 most recently registered devices, the classes recorded for TOETAL SOLUTIONS, INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TOETAL SOLUTIONS, INC in the registry?
The most recently registered devices listed for TOETAL SOLUTIONS, INC include Toetal Implant, Packaged, 3mm, 16mm T-60-0002-01, Toetal Implant, Packaged, 3mm, 18mm T-60-0002-02, Toetal Implant, Packaged, 3mm, 22mm T-60-0002-04 and Toetal Implant, Packaged, 3mm, 20mm T-60-0002-03.