Keta Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Keta Corp. makes
Keta Corp. manufactures medical devices including the QUANTUM 412, SUPERLITE PENLIGHT, and KETA HAND-HELD TONOMETER.
These devices are Class I and listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Quantum 412 Ref K844570
Regimes: 510(k) Registry: 510(k)Superlite Penlight Ref K861028
Regimes: 510(k) Registry: 510(k)Keta Hand-Held Tonometer Ref K861027
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keta Corp. have in the registry?
The registry currently lists 3 devices for Keta Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keta Corp.'s devices?
Among its 3 most recently registered devices, Keta Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Keta Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Keta Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Keta Corp. in the registry?
The most recently registered devices listed for Keta Corp. include QUANTUM 412, SUPERLITE PENLIGHT and KETA HAND-HELD TONOMETER.