Data / Medical devices / United States / Osha Review, Inc.
Osha Review, Inc.: FDA-registered device maker in Rancho Cordova, CA, United States, 1 510(k) clearance
Osha Review, Inc. is registered with the FDA (registration 3011061109) in Rancho Cordova, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 27, 1992. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3011061109
- Address
- 11306 Sunco Dr Ste 7, Rancho Cordova, CA, United States, 95742
- Owner or operator
- OSHA Review, Inc. (10047255)
- Roles
- Repackager or relabeler
- First device listed
- February 25, 2020
- Registered through
- 2027
- Brand names listed
- OSHA Review's Spore Check System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Indicator, Biological Sterilization Process | FRC | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| March 27, 1992 | K905425 | SPORVIEW | FRC | Substantially Equivalent | Spsmedical Supply Corp. | accessdata.fda.gov |
Compare with other makers
Updated March 27, 1992. 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.