Theradapt Products Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3005673742
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Theradapt Highchair/Stroller Insert Ref K942397
Regimes: 510(k) Registry: 510(k)Chairs Ref K926025
Regimes: 510(k) Registry: 510(k)Benches Ref K926028
Regimes: 510(k) Registry: 510(k)Desks Ref K926026
Regimes: 510(k) Registry: 510(k)Theradapt(R) Adjustable Classroom Chair Ref K930520
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3005673742
- Address
- 922 N WASHINGTON AVE, Ludington, MI, 49431
Frequently asked questions
How many devices does THERADAPT PRODUCTS INC. have in the registry?
The registry currently lists 5 devices for THERADAPT PRODUCTS INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list THERADAPT PRODUCTS INC.'s devices?
Among its 5 most recently registered devices, THERADAPT PRODUCTS INC. has devices listed in FDA 510(k) (5 devices).
What risk classes do THERADAPT PRODUCTS INC.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for THERADAPT PRODUCTS INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from THERADAPT PRODUCTS INC. in the registry?
The most recently registered devices listed for THERADAPT PRODUCTS INC. include THERADAPT HIGHCHAIR/STROLLER INSERT, CHAIRS, BENCHES and DESKS.