Teknomed, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Teknomed, Inc. makes
Teknomed, Inc. manufactures laser systems including the Multilase 2500 A, Multilase 2100 A, Technomed Pulsolith 4000 Laser System, Technomed Pulsolith Laser System, and Tecnotomo devices, as well as variants such as the Multilase 2100 C and 2100 D.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Multilase 2500 A Ref K920708
Regimes: 510(k) Registry: 510(k)Multilase 2100 A Ref K913290
Regimes: 510(k) Registry: 510(k)Technomed Pulsolith 4000 Laser System Ref K925395
Regimes: 510(k) Registry: 510(k)Technomed Pulsolith Laser System Ref K890436
Regimes: 510(k) Registry: 510(k)Technomed Pulsolith Laser System Ref K895178
Regimes: 510(k) Registry: 510(k)Tecnotomo Ref K790132
Regimes: 510(k) Registry: 510(k)Multilase 2100 C, 2100 D Ref K913917
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teknomed, Inc. have in the registry?
The registry currently lists 7 devices for Teknomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teknomed, Inc.'s devices?
Among its 7 most recently registered devices, Teknomed, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Teknomed, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Teknomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teknomed, Inc. in the registry?
The most recently registered devices listed for Teknomed, Inc. include MULTILASE 2500 A, MULTILASE 2100 A, TECHNOMED PULSOLITH 4000 LASER SYSTEM and TECHNOMED PULSOLITH LASER SYSTEM.