Martin S. Knopf Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Martin S. Knopf Assoc., Inc. makes
Martin S. Knopf Assoc., Inc. manufactures the H55 hydrophilic contact lens and the URAM ophthalmic laser endoscope.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
H55 Hydrophilic Contact Lens Ref K942214
Regimes: 510(k) Registry: 510(k)Uram Ophthalmic Laser Endoscope Ref K910532
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Martin S. Knopf Assoc., Inc. have in the registry?
The registry currently lists 2 devices for Martin S. Knopf Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Martin S. Knopf Assoc., Inc.'s devices?
Among its 2 most recently registered devices, Martin S. Knopf Assoc., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Martin S. Knopf Assoc., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Martin S. Knopf Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Martin S. Knopf Assoc., Inc. in the registry?
The most recently registered devices listed for Martin S. Knopf Assoc., Inc. include H55 HYDROPHILIC CONTACT LENS and URAM OPHTHALMIC LASER ENDOSCOPE.