Minvasive Devices, Inc.
Country not established
- Devices
- 1
What Minvasive Devices, Inc. makes
Minvasive Devices, Inc. manufactures laparoscopic instruments designed for minimally invasive surgical procedures, including trocars, graspers, and dissection tools. These instruments are engineered for precision in abdominal and pelvic surgeries, supporting procedures such as cholecystectomy, hernia repair, and gynecological interventions. The portfolio includes reusable and single-use devices optimized for ergonomic handling and tissue manipulation.
The company’s laparoscopic instruments fall under FDA Class II regulatory classification, requiring premarket notification (510(k)) clearance before commercial distribution in the US. These devices are listed in the FDA’s 510(k) database, reflecting their authorized status for sale in the United States. The manufacturer operates from the US, adhering to domestic regulatory requirements for medical device compliance.
Catalogue
Minivasive Laparoscopy Instruments Ref K923547
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Minvasive Devices, Inc. have in the registry?
The registry currently lists 1 device for Minvasive Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minvasive Devices, Inc.'s devices?
Among its 1 most recently registered device, Minvasive Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Minvasive Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Minvasive Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Minvasive Devices, Inc. in the registry?
The most recently registered devices listed for Minvasive Devices, Inc. include MINIVASIVE LAPAROSCOPY INSTRUMENTS.