Tiller Mind Body, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000516428
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lower Bowel Evacuation System Ref K941279
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Colonic & Enema Nozzle Ref K071057
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000516428
- Address
- 10911 West Ave, San Antonio, TX, 78213
Frequently asked questions
How many devices does TILLER MIND BODY, INC. have in the registry?
The registry currently lists 3 devices for TILLER MIND BODY, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TILLER MIND BODY, INC.'s devices?
Among its 3 most recently registered devices, TILLER MIND BODY, INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do TILLER MIND BODY, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for TILLER MIND BODY, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TILLER MIND BODY, INC. in the registry?
The most recently registered devices listed for TILLER MIND BODY, INC. include LOWER BOWEL EVACUATION SYSTEM, LIBBE RECTAL TUBE (FORMERLY A YANKAUER SUCTION TUBE) and COLONIC & ENEMA NOZZLE.