Precision Optics Corp.
United Statesfrom the FDA registration address FDA establishment FEI 1000120916
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Precision Optics Corp. makes
PRECISION OPTICS CORP. manufactures medical devices including the PRECISION OPTICS CORPORATION VIDEO OPHTHALMOSCOPE, MODEL 2500-VOS, POC ENT ENDOSCOPE - SINUSCOPE, and POC ARTHROSCOPE AND ACCESSORIES.
The company's devices are Class II and listed in the FDA 510(k) registry. PRECISION OPTICS CORP. is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Poc Ent Endoscope - Sinuscope Ref K983123
Regimes: 510(k) Registry: 510(k)Poc Arthroscope And Accessories Ref K945684
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000120916
- Address
- 22 E Broadway, GARDNER, MA, 01440
Frequently asked questions
How many devices does PRECISION OPTICS CORP. have in the registry?
The registry currently lists 3 devices for PRECISION OPTICS CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PRECISION OPTICS CORP.'s devices?
Among its 3 most recently registered devices, PRECISION OPTICS CORP. has devices listed in FDA 510(k) (3 devices).
What risk classes do PRECISION OPTICS CORP.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for PRECISION OPTICS CORP.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PRECISION OPTICS CORP. in the registry?
The most recently registered devices listed for PRECISION OPTICS CORP. include PRECISION OPTICS CORPORATION VIDEO OPHTHALMOSCOPE, MODEL 2500-VOS, POC ENT ENDOSCOPE - SINUSCOPE and POC ARTHROSCOPE AND ACCESSORIES.