Puricore, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 10
What Puricore, Inc. makes
Puricore, Inc. makes wound care and endodontic cleansing products, including the Vashe Wound Therapy System, Vashe Wound Cleansing System, Vashe Wound Solution in various sizes, Vashe Skin and Wound Hydrogel, Puricore Wound Hydrogel Spray Dressing, Sterilox Liquid Chemical Sterilant System, and Aquatine EC Endodontic Cleanser.
These devices are classified as Class II, U and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Aquatine Ec Endodontic Cleanser Ref K061689
510(k) 510(k)Vashe Wound Therapy System Model: 9000-0014 Ref K100918
510(k) 510(k)Sterilox Liquid Chemical Sterilant System Ref K063159
510(k) 510(k)Vashe Wound Therapy Solution Ref K123072
510(k) 510(k)Puricore Wound Hydrogel Spray Dressing Ref K141863
510(k) 510(k)Vashe Wound Cleansing System Ref K093155
510(k) 510(k)- 510(k) 510(k)
Vashe Skin And Wound Hydrogel Ref K123071
510(k) 510(k)Vashe Wound Therapy Solution Ref K093697
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Puricore, Inc. have in the registry?
The registry currently lists 10 devices for Puricore, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Puricore, Inc.'s devices?
Among its 10 most recently registered devices, Puricore, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Puricore, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Puricore, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Puricore, Inc. in the registry?
The most recently registered devices listed for Puricore, Inc. include AQUATINE EC ENDODONTIC CLEANSER, VASHE WOUND THERAPY SYSTEM MODEL: 9000-0014, STERILOX LIQUID CHEMICAL STERILANT SYSTEM and VASHE WOUND THERAPY SOLUTION.