Tessile, Inc.
Country not established
- Devices
- 1
What Tessile, Inc. makes
Tessile, Inc. manufactures patient examination gloves, designed for single-use medical procedures requiring barrier protection and tactile sensitivity.
These gloves are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K905172
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tessile, Inc. have in the registry?
The registry currently lists 1 device for Tessile, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tessile, Inc.'s devices?
Among its 1 most recently registered device, Tessile, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tessile, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tessile, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tessile, Inc. in the registry?
The most recently registered devices listed for Tessile, Inc. include PATIENT EXAMINATION GLOVES.