Data / Medical devices / United States / Optical Integrity, Inc.
Optical Integrity, Inc.: FDA-registered device maker in P C Beach, FL, United States, 1 510(k) clearance
Optical Integrity, Inc. is registered with the FDA (registration 3003708273) in P C Beach, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 16, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003708273
- Address
- 19408 Panama City Beach Pkwy, P C Beach, FL, United States, 32413
- Owner or operator
- OPTICAL INTEGRITY, INC. (9051267)
- Roles
- Manufacturer, Specification developer
- First device listed
- May 20, 2002
- Registered through
- 2026
- Brand names listed
- OPTICAL INTEGRITY G
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 16, 2002 | K022338 | OPTICAL INTEGRITY GENERAL SHAPED FIBER | GEX | Substantially Equivalent | Optical Integrity, Inc. | accessdata.fda.gov |
Compare with other makers
Updated October 16, 2002. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.