Data / Medical devices / United States / Cosmed Usa, Inc.
Cosmed Usa, Inc.: FDA-registered device maker in Concord, CA, United States, 2 510(k) clearances
Cosmed Usa, Inc. is registered with the FDA (registration 3003873943) in Concord, CA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 27, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003873943
- Address
- 1850 Bates Ave, Concord, CA, United States, 94520
- Owner or operator
- COSMED USA, INC. (9085998)
- Roles
- Manufacturer
- First device listed
- January 24, 2011
- Registered through
- 2026
- Brand names listed
- BOD POD, PEA POD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Plethysmograph, Air Displacement For Body Composition Analysis | OAC | 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 |
|---|---|---|---|---|---|---|
| June 27, 2006 | K060848 | BOD POD | OAC | Substantially Equivalent | Life Measurement, Inc. | accessdata.fda.gov |
| March 1, 2004 | K032610 | MODIFIED SONAMET BODY COMPOSITION ANALYZER | OAC | Substantially Equivalent | Life Measurement, Inc. | accessdata.fda.gov |
Updated June 27, 2006. 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.