Data / Medical devices / China / Cosmo Far East Technology Limited
Cosmo Far East Technology Limited: FDA-registered device maker in Shenzhen Guangdong, China, 5 510(k) clearances
Cosmo Far East Technology Limited is registered with the FDA (registration 3013519365) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated October 22, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013519365
- Address
- 3F Building 11, Section B of Xue Zi Wei Industrial Park, Shajing Street Bao an District, Shenzhen Guangdong, China, 518105
- Owner or operator
- Cosmo Far East Technology Limited (10054725)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- April 19, 2017
- Registered through
- 2026
- Brand names listed
- C244HC HairClub Advance, C304HC HairClub Premium, Diode Laser Cap: COSMO-302, COSMO-312, COSMO-272, COSMO-152, C154HC HairClub Essential,, Hair Growth Laser Cap, HairMax Laser Model 272, Model 202, and Model 80, C154HC, C244HC, C304HC, Illumiflow Laser Cap, KIIERR-302, KIIERR-272, KIIERR-148
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laser, Comb, Hair | OAP | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| October 22, 2025 | K252325 | Hair Growth Laser Cap | OAP | Substantially Equivalent | Cosmo Far East Technology Limited | accessdata.fda.gov |
| September 5, 2018 | K181878 | Kiierr 272 Laser, Kiierr 148 Laser | OAP | Substantially Equivalent | Kiierr International, LLC | accessdata.fda.gov |
| June 20, 2018 | K180885 | HairMax Laser | OAP | Substantially Equivalent | Lexington International, LLC | accessdata.fda.gov |
| February 28, 2018 | K173678 | Diode Laser Cap | OAP | Substantially Equivalent | Cosmo Far East Technology Limited | accessdata.fda.gov |
| February 24, 2017 | K162071 | IllumiFlow Laser Cap | OAP | Substantially Equivalent | Eglobal, LLC | accessdata.fda.gov |
Compare with other makers
Updated October 22, 2025. 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.