Centricity Vision, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3011398014
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
ZeptoLink IOL Positioning System Ref K223763
Regimes: 510(k) Registry: 510(k)ZEPTO Precision Capsulotomy System Ref K221188
Regimes: 510(k) Registry: 510(k)ZEPTO Precision Capsulotomy System Ref K210827
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011398014
- Address
- 1939 Palomar Oaks Way, Carlsbad, CA, 92011
Frequently asked questions
How many devices does Centricity Vision, Inc. have in the registry?
The registry currently lists 3 devices for Centricity Vision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Centricity Vision, Inc.'s devices?
Among its 3 most recently registered devices, Centricity Vision, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Centricity Vision, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Centricity Vision, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Centricity Vision, Inc. in the registry?
The most recently registered devices listed for Centricity Vision, Inc. include ZeptoLink IOL Positioning System and ZEPTO Precision Capsulotomy System.