Lasersight Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Lasersight Technologies, Inc. makes
Lasersight Technologies, Inc. manufactures ophthalmic surgical devices including ULTRAEDGE KERATOME BLADE, AUTOMATED DISPOSABLE KERATOME, ULTRASHAPER KERATOME, LASERSCAN LSX EXCIMER LASER, and KREMER LASER SYSTEM.
The company's portfolio includes Class I and Class III medical devices listed in the FDA 510(k) and FDA PMA registries. Lasersight Technologies is based in the US.
Catalogue
Ultraedge Keratome Blade, Model 374803 - Acs Ref K001144
Regimes: 510(k) Registry: 510(k)Automated Disposable Keratome (Adk) Ref K974004
Regimes: 510(k) Registry: 510(k)Ultrashaper Keratome Ref K990227
Regimes: 510(k) Registry: 510(k)Laserscan Lsx Excimer Laser Ref P980008
Regimes: PMA Registry: PMAKremer Laser System Ref P970005
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Lasersight Technologies, Inc. have in the registry?
The registry currently lists 5 devices for Lasersight Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lasersight Technologies, Inc.'s devices?
Among its 5 most recently registered devices, Lasersight Technologies, Inc. has devices listed in FDA 510(k) (3 devices) and FDA PMA (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Lasersight Technologies, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Lasersight Technologies, Inc.'s devices are Class I and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Lasersight Technologies, Inc. in the registry?
The most recently registered devices listed for Lasersight Technologies, Inc. include ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS, AUTOMATED DISPOSABLE KERATOME (ADK), ULTRASHAPER KERATOME and LASERSCAN LSX EXCIMER LASER.