Steriltx (USA), Inc.
Country not established
- Devices
- 1
What Steriltx (USA), Inc. makes
Steriltx (USA), Inc. manufactures non-chlorinated, powder-free medical gloves designed for single-use in clinical and procedural settings. These gloves are intended to provide barrier protection against pathogens and contaminants during patient care or medical procedures.
The company’s product portfolio is classified under Class I medical devices in the U.S. and is listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Stermed Non-Chlorinated Powder Free Gloves Ref K943839
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Steriltx (Usa), Inc. have in the registry?
The registry currently lists 1 device for Steriltx (Usa), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Steriltx (Usa), Inc.'s devices?
Among its 1 most recently registered device, Steriltx (Usa), Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Steriltx (Usa), Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Steriltx (Usa), Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Steriltx (Usa), Inc. in the registry?
The most recently registered devices listed for Steriltx (Usa), Inc. include STERMED NON-CHLORINATED POWDER FREE GLOVES.