# Iop, Inc.

- Location (FDA's records): Costa Mesa, CA
- FDA decisions: 9 (1989–2009): 9 510(k) clearances
- Product codes: KYF (3), MML (2), NXM (2), NFM (1), HPZ (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cook Biotech, Inc.: 4 (https://510kreport.com/company/cook-biotech)
- Bio-Tissue, Inc.: 1 (https://510kreport.com/company/bio-tissue)

## Firms that cite its devices most
- Corneat Vision, Ltd.: 1 (https://510kreport.com/company/corneat-vision)
- Innovia, LLC: 1 (https://510kreport.com/company/innovia)
- Innovative Ophthalmic Products, Inc. (Iop): 1 (https://510kreport.com/company/innovative-ophthalmic-products-iop)

## Its most-cited devices
- K062252: MOLTENO3 (2006), cited by 1
- K010852: Osmed Tissue Expander (2001), cited by 1
- K053622: Surgisis Ocular Graft (2006), cited by 1
- K090078: Kerasys Bioengineered Lamellar Patch Graft (2009), cited by 1

## Recent decisions
- K090078: Kerasys Bioengineered Lamellar Patch Graft (May 8, 2009)
- K062252: MOLTENO3 (Sep 27, 2006)
- K053622: Surgisis Ocular Graft (Mar 15, 2006)
- K010852: Osmed Tissue Expander (Aug 13, 2001)
- K003646: Suturegroove Weight Sizing Set (Feb 22, 2001)
- K994289: Suturegroove (Apr 17, 2000)
- K972143: Moa Bone / M-Sphere (Oct 16, 1997)
- K902489: Modified Molteno (TM) Implants (Aug 14, 1990)

Source page: https://510kreport.com/company/iop