Data / Medical devices / United States / Amplim, LLC
Amplim, LLC: FDA-registered device maker in San Francisco, CA, United States, 1 510(k) clearance
Amplim, LLC is registered with the FDA (registration 3013481815) in San Francisco, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 15, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013481815
- Address
- 1050 North Point #1605, San Francisco, CA, United States, 94109
- Owner or operator
- Amplim, LLC (10053773)
- Roles
- Specification developer
- First device listed
- January 10, 2017
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 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 |
|---|---|---|---|---|---|---|
| October 15, 2013 | K130231 | NON-CONTACT INFRARED THERMOMETER | FLL | Substantially Equivalent | Jinxinbao Electronic Co.,Ltd | accessdata.fda.gov |
Compare with other makers
Updated October 15, 2013. 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.