Devmed Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Devmed Corp. makes
Devmed Corp. manufactures reusable endoscopic lens wash sheaths, including specialized versions for laparoscopic procedures, and a stepping and stabilizing system designed for surgical assistance. These products are intended for use in medical settings to support endoscope reprocessing and intraoperative stability.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed via the 510(k) clearance pathway. Devices are based in the United States and comply with applicable US medical device regulations.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Devmed Stepping And Stabilizing System Ref K972152
Regimes: 510(k) Registry: 510(k)Devmed Lens Wash Sheath Ref K925669
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Devmed Corp. have in the registry?
The registry currently lists 3 devices for Devmed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Devmed Corp.'s devices?
Among its 3 most recently registered devices, Devmed Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Devmed Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Devmed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Devmed Corp. in the registry?
The most recently registered devices listed for Devmed Corp. include DEVMED LAP WASH REUSABLE ENDOSCOPIC LENS WASH SHEATH, DEVMED STEPPING AND STABILIZING SYSTEM and DEVMED LENS WASH SHEATH.