Care-Pro Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Care-Pro Industries, Inc. makes
Care-Pro Industries, Inc. manufactures single-use surgeon’s gloves and non-sterile patient examination gloves designed for medical and clinical procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Surgeon's Gloves Ref K892495
Regimes: 510(k) Registry: 510(k)Non-Sterile Patient Examination Gloves Ref K892772
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Care-Pro Industries, Inc. have in the registry?
The registry currently lists 2 devices for Care-Pro Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Care-Pro Industries, Inc.'s devices?
Among its 2 most recently registered devices, Care-Pro Industries, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Care-Pro Industries, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Care-Pro Industries, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Care-Pro Industries, Inc. in the registry?
The most recently registered devices listed for Care-Pro Industries, Inc. include SURGEON'S GLOVES and NON-STERILE PATIENT EXAMINATION GLOVES.