Dr. Collins, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Dr. Collins, Inc. makes
Dr. Collins, Inc. manufactures dental products, including Restore Toothpaste and BioMin Restore Plus, which are designed for remineralization and cavity prevention in dental care.
These products are classified as Class II medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Restore Toothpaste Ref K181965
510(k) 510(k)BioMin Restore Plus Ref K200077
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Collins, Inc. have in the registry?
The registry currently lists 2 devices for Dr. Collins, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Collins, Inc.'s devices?
Among its 2 most recently registered devices, Dr. Collins, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dr. Collins, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dr. Collins, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Collins, Inc. in the registry?
The most recently registered devices listed for Dr. Collins, Inc. include Restore Toothpaste and BioMin Restore Plus.