Data / Medical devices / United States / Itg-Medev, Inc.
Itg-Medev, Inc.: FDA-registered device maker in San Francisco, CA, United States, 1 510(k) clearance
Itg-Medev, Inc. is registered with the FDA (registration 2951555) in San Francisco, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 22, 1988. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2951555
- FEI number
- 1000307251
- Address
- 310 Arballo Dr Apt 9L, San Francisco, CA, United States, 94132
- Owner or operator
- ITG-MEDEV, INC. (9052309)
- Roles
- Specification developer
- First device listed
- June 6, 2011
- Registered through
- 2026
- Brand names listed
- Omiderm
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Occlusive | NAD | 1 | 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 |
|---|---|---|---|---|---|---|
| February 22, 1988 | K874480 | MODIFIED MANUFACTURING PROCESS FOR OMIDERM(TM) | NAD | Substantially Equivalent for Some Indications | Omikron Scientific, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 22, 1988. 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.