Cytocare, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Cytocare, Inc. makes
Cytocare, Inc. manufactures electrosurgical and laser-based medical devices for urological and endoscopic procedures, including monopolar electrodes, cryotherapy systems, and laser catheters. Their portfolio includes advanced laser delivery systems, electrosurgical handpieces, and diode laser systems designed for tissue ablation and treatment.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. These products are intended for use in the United States, where they are subject to FDA oversight.
Catalogue
Endocare Monopolar Electrodes (Modification) Ref K954321
510(k) 510(k)- 510(k) 510(k)
Endocare Monopolar Electrodes Ref K952587
510(k) 510(k)Endocare Cryotherapy System Ref K942299
510(k) 510(k)Cytocare Laser Catheter For Urology Ref K921708
510(k) 510(k)Endocare Electrosurgical Handpiece Ref K952698
510(k) 510(k)Cytocare Diode Laser System Ref K934211
510(k) 510(k)
Frequently asked questions
How many devices does Cytocare, Inc. have in the registry?
The registry currently lists 7 devices for Cytocare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cytocare, Inc.'s devices?
Among its 7 most recently registered devices, Cytocare, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Cytocare, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Cytocare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cytocare, Inc. in the registry?
The most recently registered devices listed for Cytocare, Inc. include ENDOCARE MONOPOLAR ELECTRODES (MODIFICATION), ENDOCARE PROLASE I ADVANCED LASER DELIVERY SYSTEM, ENDOCARE MONOPOLAR ELECTRODES and ENDOCARE CRYOTHERAPY SYSTEM.