Iop, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
What Iop, Inc. makes
Iop, Inc. makes ophthalmic and tissue-related medical devices including the Molteno implant and its modified versions, the SutureGroove weight sizing set, the Osmed tissue expander, the Kerasys bioengineered lamellar patch graft, the Surgisis ocular graft, and the MOA bone/M-sphere device.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Molteno Implant Ref K890598
Regimes: 510(k) Registry: 510(k)Suturegroove Ref K994289
Regimes: 510(k) Registry: 510(k)Osmed Tissue Expander Ref K010852
Regimes: 510(k) Registry: 510(k)Modified Molteno(Tm) Implants Ref K902489
Regimes: 510(k) Registry: 510(k)Kerasys Bioengineered Lamellar Patch Graft Ref K090078
Regimes: 510(k) Registry: 510(k)Surgisis Ocular Graft Ref K053622
Regimes: 510(k) Registry: 510(k)Suturegroove Weight Sizing Set Ref K003646
Regimes: 510(k) Registry: 510(k)MOLTENO3 Ref K062252
Regimes: 510(k) Registry: 510(k)Moa Bone / M-Sphere Ref K972143
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iop, Inc. have in the registry?
The registry currently lists 9 devices for Iop, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iop, Inc.'s devices?
Among its 9 most recently registered devices, Iop, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Iop, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Iop, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iop, Inc. in the registry?
The most recently registered devices listed for Iop, Inc. include MOLTENO IMPLANT, SUTUREGROOVE, OSMED TISSUE EXPANDER and MODIFIED MOLTENO(TM) IMPLANTS.