Kay Borch A/S
Country not established
- Devices
- 1
What Kay Borch A/S makes
Kay Borch A/S manufactures single-use, disposable surgical drapes and gowns designed for sterile barrier protection in operating rooms and procedural settings. These products are intended to isolate the surgical site and maintain a sterile field during invasive procedures, including general surgery, orthopedics, and minimally invasive techniques.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. regulatory requirements. Kay Borch A/S operates from the United States.
Catalogue
P1OP2B Or P1O92T Ref K954674
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kay Borch A/S have in the registry?
The registry currently lists 1 device for Kay Borch A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kay Borch A/S's devices?
Among its 1 most recently registered device, Kay Borch A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Kay Borch A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kay Borch A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kay Borch A/S in the registry?
The most recently registered devices listed for Kay Borch A/S include P1OP2B OR P1O92T.