Ophthalmic Consultants, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ophthalmic Consultants, Inc. makes
Ophthalmic Consultants, Inc. manufactures scleral plugs in 19 and 20 gauge sizes for ocular applications, as well as irrigation/aspiration (I/A) surgical packs for procedures including posterior vitrectomy, anterior vitrectomy, phacoemulsification, and administration-related uses.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Scleral Plugs, 19 And 20 Gauge Ref K990872
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ophthalmic Consultants, Inc. have in the registry?
The registry currently lists 2 devices for Ophthalmic Consultants, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ophthalmic Consultants, Inc.'s devices?
Among its 2 most recently registered devices, Ophthalmic Consultants, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ophthalmic Consultants, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ophthalmic Consultants, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ophthalmic Consultants, Inc. in the registry?
The most recently registered devices listed for Ophthalmic Consultants, Inc. include SCLERAL PLUGS, 19 AND 20 GAUGE and I/A (IRRIGATION/ASPIRATION) PACK, POSTERIOR VITRECOMY PACK, ANTERIOR VIRECTOMY PACK, PHACOEMULSIFICATION PACK, ADMIINISN.