Invamed, Inc.
United Statesfrom the FDA registration address FDA FEI 3041846470
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Invamed, Inc. makes
Invamed, Inc. manufactures reusable laparoscopic trocar systems designed for minimally invasive surgical procedures, facilitating instrument insertion and gas insufflation in abdominal surgeries.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Invamed Reusable Laparoscopic Trocar System Ref K936011
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3041846470
- Address
- One World Trade Center 285 Fulton St.85th Floor New York, NY 10007, New York, NY, 10007
Frequently asked questions
How many devices does Invamed, Inc. have in the registry?
The registry currently lists 1 device for Invamed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Invamed, Inc.'s devices?
Among its 1 most recently registered device, Invamed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Invamed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Invamed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Invamed, Inc. in the registry?
The most recently registered devices listed for Invamed, Inc. include INVAMED REUSABLE LAPAROSCOPIC TROCAR SYSTEM.