Data / Medical devices / United States / Apira Science, Inc.
Apira Science, Inc.: FDA-registered device maker in Albuquerque, NM, United States, 4 510(k) clearances
Apira Science, Inc. is registered with the FDA (registration 3009118729) in Albuquerque, NM, United States. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated December 2, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009118729
- Address
- 409 Edmon Rd. NE Suite C, Albuquerque, NM, United States, 87107
- Owner or operator
- Apira Science, Inc. (10043658)
- Roles
- Manufacturer
- First device listed
- March 8, 2013
- Registered through
- 2026
- Brand names listed
- GroWell BT hair growth system, iGrow
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laser, Comb, Hair | OAP | 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 |
|---|---|---|---|---|---|---|
| December 2, 2024 | K242619 | GroWell BT Hair Growth System (GW10042) | OAP | Substantially Equivalent | Apira Science, Inc. | accessdata.fda.gov |
| December 5, 2014 | K140931 | IGROW II HAIR GROWTH SYSTEM | OAP | Substantially Equivalent | Apira Science, Inc. | accessdata.fda.gov |
| August 21, 2014 | K141567 | IGROW - II HAIR GROWTH SYSTEM, IGROW HAIR GROWTH SYSTEM | OAP | Substantially Equivalent | Apira Science, Inc. | accessdata.fda.gov |
| December 5, 2012 | K122248 | IGROW II HAIR GROWTH SYSTEM | OAP | Substantially Equivalent | Apira Science, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 2, 2024. 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.