Pelikan Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pelikan Technologies, Inc. makes
Pelikan Technologies, Inc. makes the L1-PRO System and the L1 System.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
L1-Pro System Ref K041665
Regimes: 510(k) Registry: 510(k)L1 System Ref K024170
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pelikan Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Pelikan Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pelikan Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Pelikan Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pelikan Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pelikan Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pelikan Technologies, Inc. in the registry?
The most recently registered devices listed for Pelikan Technologies, Inc. include L1-PRO SYSTEM and L1 SYSTEM.