Data / Medical devices / United States / Carelife (usa) Inc.
Carelife (usa) Inc.: FDA-registered device maker in Alpharetta, GA, United States, 1 510(k) clearance
Carelife (usa) Inc. is registered with the FDA (registration 3010481217) in Alpharetta, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 26, 2021. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3010481217
- Address
- 1120 Alpha Dr., Alpharetta, GA, United States, 30004
- Owner or operator
- CARELIFE USA INC (10045614)
- Roles
- Specification developer
- First device listed
- July 13, 2026
- Registered through
- 2027
- Brand names listed
- RG3
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Pump, Infusion | MRZ | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| March 26, 2021 | K201634 | RG 3ml Medication Cartridge | MRZ | Substantially Equivalent | Chengdu Shifeng Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 26, 2021. 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.