Data / Medical devices / United States / Meditherm Inc.
Meditherm Inc.: FDA-registered device maker in Albuquerque, NM, United States, 1 510(k) clearance
Meditherm Inc. is registered with the FDA (registration 3006111110) in Albuquerque, NM, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 21, 2001. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006111110
- Address
- 5353 Wyoming BLVD NE Suite D, Albuquerque, NM, United States, 87108
- Owner or operator
- MEDITHERM INC. (9096265)
- Roles
- Manufacturer
- First device listed
- January 4, 2007
- Registered through
- 2026
- Brand names listed
- FS 520, IRIS 160, IRIS 200, IRIS 400, MED2000, MED2000 IRIS, MED2000 IRIS Elite, MED2000 Pro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Telethermographic (Adjunctive Use) | LHQ | 1 | 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 |
|---|---|---|---|---|---|---|
| February 21, 2001 | K003332 | MEDITHERM MED2000 | LHQ | Substantially Equivalent | Meditherm, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 21, 2001. 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.