R. Thomas Grotz, M.D., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does R. Thomas Grotz, M.D., Inc. have in the registry?
The registry currently lists 4 devices for R. Thomas Grotz, M.D., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list R. Thomas Grotz, M.D., Inc.'s devices?
Among its 4 most recently registered devices, R. Thomas Grotz, M.D., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do R. Thomas Grotz, M.D., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for R. Thomas Grotz, M.D., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from R. Thomas Grotz, M.D., Inc. in the registry?
The most recently registered devices listed for R. Thomas Grotz, M.D., Inc. include STABILIZER SOFT TISSUE ANCHOR, 8MM MODEL TA1008, ANCHOR INSERTER/SUTURE ORGANIZER, 8MM MODEL AI1008, STABILIZER DRILL, 8, STABILIZER SOFT TISSUE ANCHOR MODEL NUMBER TA1005, TA1008, ANCHOR INSERTER/SUTURE ORGANIZER MODEL NUMBERS AI1005, AI1008, STABILIZER SOFT TISSUE ANCHOR 5MM MODEL TA1005, ANCHOR INSERTER/SUTURE ORGANIZER 5MM AI1005, STABILIZER DRILL 5MM NONSTE and STABILIZER SOFT TISSUE ANCHOR, 5 AND 8MM; ANCHOR INSERTER, 5 AND 8MM; STABILIZER DRILL, 5 AND 8MM, NONSTERILE; STABILIZE.