Assure Tech LLC
United Statesfrom the FDA registration address FDA establishment FEI 3030648160
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
AssureTech Quick Cup Tests Ref K261984
Regimes: 510(k) Registry: 510(k)Fastep COVID-19 Antigen Pen Home Test Ref K260754
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3030648160
- Address
- 1521 Concord Pike Suite 201, Wilmington, DE, 19803
Frequently asked questions
How many devices does ASSURE TECH LLC have in the registry?
The registry currently lists 10 devices for ASSURE TECH LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list ASSURE TECH LLC's devices?
Among its 10 most recently registered devices, ASSURE TECH LLC has devices listed in FDA 510(k) (10 devices).
What risk classes do ASSURE TECH LLC's devices fall under?
Among its 10 most recently registered devices, the classes recorded for ASSURE TECH LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ASSURE TECH LLC in the registry?
The most recently registered devices listed for ASSURE TECH LLC include AssureTech Quick Cup Tests, Fastep COVID-19 Antigen Pen Home Test, AssureTech Secobarbital Strip, AssureTech Oxycodone Strip, AssureTech Secobarbital/Oxycodone Panel Dip, AssureTech Secobarbital/Oxycodone Quick Cup, AssureTech Secobarbital/Oxycodone Turn Key-Split Cup and Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test Strip.