The Jerome Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What The Jerome Group, Inc. makes
The Jerome Group, Inc. manufactures orthopedic fixation devices, including glass rings for surgical applications and ceramic-tipped skull pins used in cranial stabilization procedures.
These products fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Jerome Glass Ring Ref K023959
Regimes: 510(k) Registry: 510(k)Ceramic Tipped Skull Pin Ref K040363
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Jerome Group, Inc. have in the registry?
The registry currently lists 2 devices for The Jerome Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Jerome Group, Inc.'s devices?
Among its 2 most recently registered devices, The Jerome Group, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Jerome Group, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Jerome Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Jerome Group, Inc. in the registry?
The most recently registered devices listed for The Jerome Group, Inc. include JEROME GLASS RING and CERAMIC TIPPED SKULL PIN.