Tek-Aid, Inc.
Country not established
- Devices
- 1
What Tek-Aid, Inc. makes
Tek-Aid, Inc. manufactures the Le Veen Wound Splint, a device designed to immobilize and support wounds to facilitate healing by maintaining proper alignment and reducing movement.
The Le Veen Wound Splint is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Le Veen Wound Splint Ref K863570
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tek-Aid, Inc. have in the registry?
The registry currently lists 1 device for Tek-Aid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tek-Aid, Inc.'s devices?
Among its 1 most recently registered device, Tek-Aid, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tek-Aid, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tek-Aid, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tek-Aid, Inc. in the registry?
The most recently registered devices listed for Tek-Aid, Inc. include LE VEEN WOUND SPLINT.