Vidamed, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
What Vidamed, Inc. makes
Vidamed, Inc. manufactures radiofrequency (RF) ablation systems and accessories for transurethral procedures, including disposable and reusable handpieces, cartridges, generators, and catheters. Their portfolio includes office-based TUNA (Transurethral Needle Ablation) systems, electrosurgical generators, and RF data recorders designed for prostate tissue treatment. The company also produces specialized handpieces like the Cobra handpiece and telescopes for procedural guidance.
Vidamed’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The products are listed in the FDA’s 510(k) registry, adhering to U.S. medical device compliance standards. The company operates from the United States.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Vidamed, Inc. have in the registry?
The registry currently lists 11 devices for Vidamed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vidamed, Inc.'s devices?
Among its 11 most recently registered devices, Vidamed, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Vidamed, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Vidamed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vidamed, Inc. in the registry?
The most recently registered devices listed for Vidamed, Inc. include RF GENERATORS, DISPOSABLE CARTRIDGE KIT, DISPOSABLE CARTRIDGE, REUSABLE HANDLE, DISOISABLE HANDPIECE REUSABLE TELESCOPE, COBRA HAND PIECE, TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM and VIDAMED MODEDL 7600 RF GENERATOR.