Mentor Ophthalmics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Mentor Ophthalmics, Inc. makes
Mentor Ophthalmics manufactures surgical drapes, hemostatic tools, and diagnostic instruments for ophthalmic procedures. Their products include absorbent drapes for wound protection, a hemostatic eraser for precise bleeding control, a handheld tonometer for intraocular pressure measurement, and a system for anterior chamber maintenance during cataract surgery.
The company’s portfolio consists of Class II devices, each authorised via the FDA’s 510(k) clearance process. These products are listed under the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Mentor Super Absorbent Drape Ref K973146
Regimes: 510(k) Registry: 510(k)Mentor Gemini Hemostatic Eraser Ref K971538
Regimes: 510(k) Registry: 510(k)Mentor Tono-Pen 3 Ref K964312
Regimes: 510(k) Registry: 510(k)Mentor Advent A/B System Ref K960765
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mentor Ophthalmics, Inc. have in the registry?
The registry currently lists 4 devices for Mentor Ophthalmics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mentor Ophthalmics, Inc.'s devices?
Among its 4 most recently registered devices, Mentor Ophthalmics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Mentor Ophthalmics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mentor Ophthalmics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mentor Ophthalmics, Inc. in the registry?
The most recently registered devices listed for Mentor Ophthalmics, Inc. include MENTOR SUPER ABSORBENT DRAPE, MENTOR GEMINI HEMOSTATIC ERASER, MENTOR TONO-PEN 3 and MENTOR ADVENT A/B SYSTEM.