Precision Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hessburg-Bfrron Trephine Ref K801585
Regimes: 510(k) Registry: 510(k)Ring Supported Trephine For Cornea Trans Ref K843048
Regimes: 510(k) Registry: 510(k)Barron Twin Blade Trephine For Eppikaratophakia Ref K860648
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Instruments, Inc. have in the registry?
The registry currently lists 4 devices for Precision Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Instruments, Inc.'s devices?
Among its 4 most recently registered devices, Precision Instruments, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Precision Instruments, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Precision Instruments, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Precision Instruments, Inc. in the registry?
The most recently registered devices listed for Precision Instruments, Inc. include HESSBURG-BFRRON TREPHINE, RING SUPPORTED TREPHINE FOR CORNEA TRANS, BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA and BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON.