Lincoln Diagnostics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1450391
- Devices
- 15
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 15 devicesCompany details
- FDA FEI number
- 1450391
- Address
- 240 E. HICKORY POINT RD., DECATUR, IL, 62526
Frequently asked questions
How many devices does LINCOLN DIAGNOSTICS, INC. have in the registry?
The registry currently lists 15 devices for LINCOLN DIAGNOSTICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LINCOLN DIAGNOSTICS, INC.'s devices?
Among its 15 most recently registered devices, LINCOLN DIAGNOSTICS, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LINCOLN DIAGNOSTICS, INC.'s devices fall under?
Among its 15 most recently registered devices, the classes recorded for LINCOLN DIAGNOSTICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LINCOLN DIAGNOSTICS, INC. in the registry?
The most recently registered devices listed for LINCOLN DIAGNOSTICS, INC. include Multi-Test Skin Test System MH-6, Multi-Test Skin Test System MH-6 BLK, Multi-Test II Skin Test System MH-II 6 and Duotip-Test Skin Test System LDT-100.