Nexgen Medical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
What Nexgen Medical Systems, Inc. makes
Nexgen Medical Systems, Inc. manufactures peripheral interventional devices, including guide catheters, expandable catheters, and mechanical retrieval devices available in various lengths and models.
The company's portfolio consists of Class II devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Nexgen Peripheral Guide Catheter Ref K102979
Regimes: 510(k) Registry: 510(k)Nexgen Peripheral Mechanical Retrieval Device - 200cm, Model Mrd-1000; 80 Cm, Model Mrd-2000 Ref K090932
Regimes: 510(k) Registry: 510(k)Nexgen Peripheral Mechanical Retrieval Device Ref K110315
Regimes: 510(k) Registry: 510(k)Nexgen Expandable Catheter Ref K102925
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 018652637
Frequently asked questions
How many devices does Nexgen Medical Systems, Inc. have in the registry?
The registry currently lists 9 devices for Nexgen Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nexgen Medical Systems, Inc.'s devices?
Among its 9 most recently registered devices, Nexgen Medical Systems, Inc. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Nexgen Medical Systems, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Nexgen Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nexgen Medical Systems, Inc. in the registry?
The most recently registered devices listed for Nexgen Medical Systems, Inc. include XCOIL Retractor XR100-2, XCOIL Encapsulator XE501, XCOIL Retractor XR200 and XCOIL Retractor XR100-5.