Data / Medical devices / United States / Numotech, Inc.
Numotech, Inc.: FDA-registered device maker in Northridge, CA, United States, 2 510(k) clearances
Numotech, Inc. is registered with the FDA (registration 2030595) in Northridge, CA, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 3, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2030595
- FEI number
- 1000518730
- Address
- 9420 Reseda BLVD., Suite 504, Northridge, CA, United States, 91324
- Owner or operator
- NUMOTECH, INC. (9016227)
- Roles
- Specification developer
- First device listed
- January 22, 1996
- Registered through
- 2026
- Brand names listed
- NUMOBAG, NUMOTECH BACK SUPPORT SYSTEM, TOTAL CONTACT SEAT RIPPLE SYSTEM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bed, Flotation Therapy, Powered | IOQ | 2 | Specification developer | accessdata.fda.gov |
| Chamber, Oxygen, Topical, Extremity | KPJ | 2 | Specification developer | accessdata.fda.gov |
| Cushion, Flotation | KIC | 1 | Specification developer | accessdata.fda.gov |
| Cushion, Flotation, Therapeutic | MOC | 2 | Specification developer | accessdata.fda.gov |
| Support, Head And Trunk, Wheelchair | IMS | 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 3, 1999 | K981949 | NUMOBAG | KPJ | Substantially Equivalent | Numotech, Inc. | accessdata.fda.gov |
| July 31, 1995 | K943433 | TOTAL CONTACT SEAT RIPPLE SYSTEM | IOQ | Substantially Equivalent | Numotech, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Support, Head And Trunk, Wheelchair
- All makers of Chamber, Oxygen, Topical, Extremity
- All makers of Cushion, Flotation
- All makers of Bed, Flotation Therapy, Powered
- All makers of Cushion, Flotation, Therapeutic
Updated February 3, 1999. 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.