John F. Greer Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What John F. Greer Co., Inc. makes
John F. Greer Co., Inc. manufactures medical devices including ULTRA-GEL, E-Z HOLD, E-Z LOOP, E-Z HOLD WITH ADHESIVE BASE, and EZ TAC FILTER.
These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Ultra-Gel - #4083 Ref K864189
Regimes: 510(k) Registry: 510(k)E-Z Hold - #4060 Ref K864190
Regimes: 510(k) Registry: 510(k)E-Z Loop Ref K870577
Regimes: 510(k) Registry: 510(k)E-Z Hold With Adhesive Base.-#4065 Ref K864188
Regimes: 510(k) Registry: 510(k)Ez Tac Filter Ref K870531
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does John F. Greer Co., Inc. have in the registry?
The registry currently lists 5 devices for John F. Greer Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list John F. Greer Co., Inc.'s devices?
Among its 5 most recently registered devices, John F. Greer Co., Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do John F. Greer Co., Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for John F. Greer Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from John F. Greer Co., Inc. in the registry?
The most recently registered devices listed for John F. Greer Co., Inc. include ULTRA-GEL - #4083, E-Z HOLD - #4060, E-Z LOOP and E-Z HOLD WITH ADHESIVE BASE.-#4065.