Inframed, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Inframed, Inc. makes
Inframed, Inc. manufactures laser-based medical devices, including the TT25RF for transdermal applications and the CILAS YM 101 and YM101 Nd:YAG lasers designed for neurological procedures.
Their portfolio includes Class II and Class III devices, with products authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Model TT25RF Ref K844178
Regimes: 510(k) Registry: 510(k)Cilas Ym 101 Nd:yag Laser For Neurological Use Ref K864610
Regimes: 510(k) Registry: 510(k)Cilas Model YM101 Ref K852761
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inframed, Inc. have in the registry?
The registry currently lists 3 devices for Inframed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inframed, Inc.'s devices?
Among its 3 most recently registered devices, Inframed, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Inframed, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Inframed, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Inframed, Inc. in the registry?
The most recently registered devices listed for Inframed, Inc. include MODEL TT25RF, CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE and CILAS MODEL YM101.