Data / Medical devices / United States / Valhalla Scientific, Inc.
Valhalla Scientific, Inc.: FDA-registered device maker in Poway, CA, United States, 1 510(k) clearance
Valhalla Scientific, Inc. is registered with the FDA (registration 2025475) in Poway, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 5, 1987. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2025475
- Address
- 12127 Kirkham Rd., Poway, CA, United States, 92064
- Owner or operator
- Valhalla Scientific Inc (2025475)
- Roles
- Manufacturer
- First device listed
- July 31, 2013
- Registered through
- 2027
- Brand names listed
- BCS Elite, BodyCompScale, G6 Duo, G6 Series, G6 SmartSeries
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Plethysmograph, Impedance | DSB | 2 | 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 5, 1987 | K861205 | 1990A BIO-RESISTANCE BODY COMPOSITION ANALYZER | DSB | Substantially Equivalent | Valhalla Scientific | accessdata.fda.gov |
Compare with other makers
Updated January 5, 1987. 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.