Data / Medical devices / United States / Anaerobe Systems
Anaerobe Systems: FDA-registered device maker in Morgan Hill, CA, United States, 1 510(k) clearance
Anaerobe Systems is registered with the FDA (registration 2916932) in Morgan Hill, CA, United States. It lists 9 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 31, 1984. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2916932
- Address
- 15906 Concord Circle, Morgan Hill, CA, United States, 95037
- Owner or operator
- Biolog Inc (10094615)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- December 10, 2025
- Registered through
- 2026
- Brand names listed
- ANAEROBIC TISSUE TRANSPORT8mL, ANAEROBIC TRANSPORT MEDIUM, ANAEROBIC TRANSPORT SURGERY PK, AS-150 Anaerobic Chamber, AS-500 Anaerobic Chamber, AS-580 Anaerobic Chamber, BBE QUADS, BBE SINGLES and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Anaerobic Box Glove | JTM | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, Anaerobic Transport | JSL | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, Enriched | KZI | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, General Nutrient Broth | JSC | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, Non-Selective And Differential | JSH | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, Non-Selective And Non-Differential | JSG | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, Selective And Differential | JSI | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Culture Media, Selective And Non-Differential | JSJ | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Discs, Strips And Reagents, Microorganism Differentiation | JTO | 1 | Complaint file establishment, Manufacturer | 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 |
|---|---|---|---|---|---|---|
| January 31, 1984 | K834357 | ANA TRANS TUBE & SWABS STERILE PACK | JSL | Substantially Equivalent | Anaerobe Systems | accessdata.fda.gov |
Compare with other makers
- All makers of Culture Media, General Nutrient Broth
- All makers of Culture Media, Non-Selective And Differential
- All makers of Culture Media, Anaerobic Transport
- All makers of Culture Media, Non-Selective And Non-Differential
- All makers of Discs, Strips And Reagents, Microorganism Differentiation
- All makers of Culture Media, Selective And Differential
Updated January 31, 1984. 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.