# Integrated Orbital Implants, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 5 (1989–2001): 5 510(k) clearances
- Product codes: HPZ (3), MQU (2)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kolberg Ocular Products, Inc.: 1 (https://510kreport.com/company/kolberg-ocular-products)
- Interpore Intl.: 1 (https://510kreport.com/company/interpore-intl)
- Porex Technologies Corp.: 1 (https://510kreport.com/company/porex-technologies)
- Porex Technologies Corp. of Georgia: 1 (https://510kreport.com/company/porex-technologies-of-georgia)
- Porex Surgical, Inc.: 1 (https://510kreport.com/company/porex-surgical)

## Firms that cite its devices most
- Hydron, Ltd.: 1 (https://510kreport.com/company/hydron)
- Laboratoire Villanova: 1 (https://510kreport.com/company/laboratoire-villanova)

## Its most-cited devices
- K003338: Bio-Eye II Orbital Implant (2001), cited by 1
- K891137: Motility Orbital Implant (1989), cited by 1
- K982562: Bio-Eye Hydroxyapatite Ocular Impland and Conformer (1998), cited by 1

## Recent decisions
- K003338: Bio-Eye II Orbital Implant (Feb 7, 2001)
- K000151: Perry-Kolberg (PK) HA-Coated Titanium Sleeve (Apr 10, 2000)
- K982562: Bio-Eye Hydroxyapatite Ocular Impland and Conformer (Dec 28, 1998)
- K974203: Perry-Kolberg (PK) Titanium Motility/Support System (Feb 4, 1998)
- K891137: Motility Orbital Implant (Aug 24, 1989)

Source page: https://510kreport.com/company/integrated-orbital-implants