Surgidev Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Surgidev Corp. makes
Surgidev Corp. makes ophthalmic surgical instruments including the Leading Edge Ophthalmic Knife, the Acuflo Volumetric Controlled Delivery System 2000, the Karickhoff Keratoscope, and the Karickhoff Flying Corpuscle Viewer.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Leading Edge Ophthalmic Knife Ref K831975
Regimes: 510(k) Registry: 510(k)Acuflo Volumetric Controlled Delivery Sys 2000 Ref K850729
Regimes: 510(k) Registry: 510(k)Karickhoff Keratoscope Ref K830008
Regimes: 510(k) Registry: 510(k)Karickhoff Flying Corpuscle Viewer Ref K831829
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgidev Corp. have in the registry?
The registry currently lists 4 devices for Surgidev Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgidev Corp.'s devices?
Among its 4 most recently registered devices, Surgidev Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Surgidev Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Surgidev Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgidev Corp. in the registry?
The most recently registered devices listed for Surgidev Corp. include LEADING EDGE OPHTHALMIC KNIFE, ACUFLO VOLUMETRIC CONTROLLED DELIVERY SYS 2000, KARICKHOFF KERATOSCOPE and KARICKHOFF FLYING CORPUSCLE VIEWER.