Amplim, LLC
United Statesfrom the FDA registration address FDA FEI 3013481815
Amplim, LLC is a medical device manufacturer, with 75 devices listed in FDA GUDID (FDA Class II and I) as of 14 Nov 2026.
- Devices
- 75
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 75
- Device classes
- FDA Class II 67
- FDA Class I 8
- Identifiers
- FDA FEI 3013481815
- DUNS 080521945
At a glance
Market reach
- United States
- FDA FEI
What Amplim, LLC makes
Amplim, LLC manufactures in vitro diagnostic test kits for total human chorionic gonadotropin and luteinizing hormone, both in rapid immunochromatographic formats for clinical use. The company also produces infrared skin thermometers, intermittent electronic patient thermometers, manual breast pumps, and portable automatic-inflation electronic sphygmomanometers for arm or wrist use.
These devices are classified as Class I and Class II medical devices and are listed in the FDA’s Unique Device Identification (fda_udi) registry.
Catalogue
Search and filter all 75 devicesShowing 1-50 of 75
Company details
- FDA FEI number
- 3013481815
- DUNS number
- 080521945
- Address
- 1050 North Point #1605, San Francisco, CA, 94109
Frequently asked questions
How many devices does AMPLIM, LLC have in the registry?
The registry currently lists 75 devices for AMPLIM, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list AMPLIM, LLC's devices?
Among its 50 most recently registered devices, AMPLIM, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do AMPLIM, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for AMPLIM, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from AMPLIM, LLC in the registry?
The most recently registered devices listed for AMPLIM, LLC include AMPLIM A-AMPMED-AMP1906-NA-PB, AMPLIM A-AMPMED-AMP1906-NA-BG, AMPMED AMP1701AE2 and AMPMED AMP1701W1.