Precision-Cosmet Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Precision-Cosmet Co., Inc. makes
Precision-Cosmet Co., Inc. manufactures ophthalmic surgical tools, including the Petrus IOL Guide for intraocular lens placement, the Precision-Cosmet Capsule Coupeur for lens capsule division, and manual ophthalmic surgical instruments. The company also produces the White Ocular Pressure Relief Device, designed to reduce intraocular pressure.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions supported via 510(k) clearance pathways. The company is based in the United States.
Catalogue
Petrus IOL Guide Ref K840104
Regimes: 510(k) Registry: 510(k)Precision - Cosmet Capsule Coupeur Ref K852934
Regimes: 510(k) Registry: 510(k)Manual Ophthalmic Surgical Instruments Ref K861057
Regimes: 510(k) Registry: 510(k)White Ocular Pressure Relief Device Ref K840204
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision-Cosmet Co., Inc. have in the registry?
The registry currently lists 4 devices for Precision-Cosmet Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision-Cosmet Co., Inc.'s devices?
Among its 4 most recently registered devices, Precision-Cosmet Co., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Precision-Cosmet Co., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Precision-Cosmet Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision-Cosmet Co., Inc. in the registry?
The most recently registered devices listed for Precision-Cosmet Co., Inc. include PETRUS IOL GUIDE, PRECISION - COSMET CAPSULE COUPEUR, MANUAL OPHTHALMIC SURGICAL INSTRUMENTS and WHITE OCULAR PRESSURE RELIEF DEVICE.