Kimberly-Clark Health Care
Country not established
- Devices
- 5
What Kimberly-Clark Health Care makes
Kimberly-Clark Health Care manufactures single-use sterilization wraps designed for medical device sterilization in healthcare settings, including autoclave and ethylene oxide processes. These wraps provide barrier protection to maintain sterility during storage and transport.
The company’s sterilization wraps are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. These products are registered in the U.S. and comply with relevant FDA requirements for sterile barrier systems.
Catalogue
Kimguard One-Step Sterilization Wrap Ref K141612
Regimes: 510(k) Registry: 510(k)KIMGUARD ONE-STEP Sterilization Wrap Ref K143053
Regimes: 510(k) Registry: 510(k)KIMGUARD ONE-STEP Sterilization Wrap Ref K142782
Regimes: 510(k) Registry: 510(k)Kimguard One-Step Sterilization Wrap Ref K141071
Regimes: 510(k) Registry: 510(k)Kimguard One Step Sterilization Wrap Ref K113806
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kimberly-Clark Health Care have in the registry?
The registry currently lists 5 devices for Kimberly-Clark Health Care. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kimberly-Clark Health Care's devices?
Among its 5 most recently registered devices, Kimberly-Clark Health Care has devices listed in FDA 510(k) (5 devices).
What risk classes do Kimberly-Clark Health Care's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Kimberly-Clark Health Care's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kimberly-Clark Health Care in the registry?
The most recently registered devices listed for Kimberly-Clark Health Care include KIMGUARD ONE-STEP STERILIZATION WRAP and KIMGUARD ONE STEP STERILIZATION WRAP.