Argus Medical Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Argus Medical Co., Inc. makes
Argus Medical Co., Inc. manufactures surgical instrument systems for minimally invasive procedures, including laparoscopy, arthroscopy, hysteroscopy, sinus endoscopy, and plastic surgery. Their portfolio includes dedicated systems for discetomy and endoscopic plastic surgery, designed for precision in various specialty areas.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Argus Laparoscopy Instrument System Ref K950378
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Argus Arthroscopy Instrument System Ref K950242
Regimes: 510(k) Registry: 510(k)Argus Hysteroscopy Instrument System Ref K950255
Regimes: 510(k) Registry: 510(k)Argus Sinus Endoscopy Instrument System Ref K946011
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Argus Medical Co., Inc. have in the registry?
The registry currently lists 6 devices for Argus Medical Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Argus Medical Co., Inc.'s devices?
Among its 6 most recently registered devices, Argus Medical Co., Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Argus Medical Co., Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Argus Medical Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Argus Medical Co., Inc. in the registry?
The most recently registered devices listed for Argus Medical Co., Inc. include ARGUS LAPAROSCOPY INSTRUMENT SYSTEM, ARGUS ENDOSCOPIC PLASTIC SURGERY INSTRUMENT SYSTEM, ARGUS ARTHROSCOPY INSTRUMENT SYSTEM and ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM.