Alcon Surgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Alcon Surgical, Inc. makes
Alcon Surgical, Inc. manufactures ophthalmic surgical devices, including automated hydrosonic systems for cataract surgery, retinal treatment tools, and a Class II Nd:YAG ophthalmic laser for posterior capsulotomy and iridotomy procedures.
Their portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Automated Hydrosonics(Tm) Ref K902798
Regimes: 510(k) Registry: 510(k)Retinal Taak Ref K901275
Regimes: 510(k) Registry: 510(k)Model 2800 Nd:yag Ophthalmic Laser Ref K897099
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alcon Surgical, Inc. have in the registry?
The registry currently lists 3 devices for Alcon Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alcon Surgical, Inc.'s devices?
Among its 3 most recently registered devices, Alcon Surgical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Alcon Surgical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Alcon Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alcon Surgical, Inc. in the registry?
The most recently registered devices listed for Alcon Surgical, Inc. include AUTOMATED HYDROSONICS(TM), RETINAL TAAK and MODEL 2800 ND:YAG OPHTHALMIC LASER.