Surgical Devices, Tyco Healthcare Group LP
United StatesFDA applicant, unverified
- Devices
- 2
What Surgical Devices, Tyco Healthcare Group LP makes
Surgical Devices, Tyco Healthcare Group LP manufactures absorbable wound closure devices, specifically the V-LOC 180 product line.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
V-Loc 180 Absorbable Wound Closure Device Ref K082662
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgical Devices, Tyco Healthcare Group LP have in the registry?
The registry currently lists 2 devices for Surgical Devices, Tyco Healthcare Group LP. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgical Devices, Tyco Healthcare Group LP's devices?
Among its 2 most recently registered devices, Surgical Devices, Tyco Healthcare Group LP has devices listed in FDA 510(k) (2 devices).
What risk classes do Surgical Devices, Tyco Healthcare Group LP's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Surgical Devices, Tyco Healthcare Group LP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgical Devices, Tyco Healthcare Group LP in the registry?
The most recently registered devices listed for Surgical Devices, Tyco Healthcare Group LP include V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE and MODIFICATION TO V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE.