Storz Ophthalmics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Storz Ophthalmics, Inc. makes
Storz Ophthalmics, Inc. manufactures ophthalmic devices including the STORS SCLERAL SPONGE II (LINCOFF DESIGN), MEDITEC QL-15 ND:YAG LASER, BINKHORST & FEDOROV I IRIS CLIP IOLS, and CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS.
The company's portfolio includes Class II and Class III medical devices, which are listed in the FDA 510(k) and FDA PMA registries. Storz Ophthalmics, Inc. is based in the US.
Catalogue
Stors Scleral Sponge Ii (Lincoff Design) Ref K950599
Regimes: 510(k) Registry: 510(k)Meditec Ql-15 Nd:yag Laser Ref K884060
Regimes: 510(k) Registry: 510(k)Binkhorst & Fedorov I Iris Clip IOLs Ref P800027
Regimes: PMA, withdrawn Registry: PMA- Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Storz Ophthalmics, Inc. have in the registry?
The registry currently lists 4 devices for Storz Ophthalmics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Storz Ophthalmics, Inc.'s devices?
Among its 4 most recently registered devices, Storz Ophthalmics, Inc. has devices listed in FDA 510(k) (2 devices) and FDA PMA (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Storz Ophthalmics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Storz Ophthalmics, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Storz Ophthalmics, Inc. in the registry?
The most recently registered devices listed for Storz Ophthalmics, Inc. include STORS SCLERAL SPONGE II (LINCOFF DESIGN), MEDITEC QL-15 ND:YAG LASER, BINKHORST & FEDOROV I IRIS CLIP IOLS and CHOYCE MARK VIII ANTERIOR CHAMBER INTEROCULAR LENS.