IVD Research, LLC.
United Statesfrom the FDA registration address FDA establishment FEI 3002023342
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Ivd Giardia Antigen Detection Assay Model Gl-96 Ref K020583
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Ivd Crypto/Giardia Dfa Ref K024113
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3002023342
- Address
- 5909 SEA LION PLACE, SUITE D, Carlsbad, CA, 92010
Frequently asked questions
How many devices does IVD RESEARCH, LLC. have in the registry?
The registry currently lists 9 devices for IVD RESEARCH, LLC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list IVD RESEARCH, LLC.'s devices?
Among its 9 most recently registered devices, IVD RESEARCH, LLC. has devices listed in FDA 510(k) (5 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do IVD RESEARCH, LLC.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for IVD RESEARCH, LLC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from IVD RESEARCH, LLC. in the registry?
The most recently registered devices listed for IVD RESEARCH, LLC. include Cryptosporidium Stool Antigen Detection Assay CP2-96, Giardia/Cryptosporidium Antigen Detection Assay CP/GL-96, Giardia Stool Antigen Detection Assay GL2-96 and Crypto/Giardia Human Fecal Direct Fluorescent Antigen Detection Kit C/G-DFA.