Mid-American Dental Specialties, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Mid-American Dental Specialties, Inc. makes
Mid-American Dental Specialties, Inc. manufactures orthodontic brackets, including the RegenCy Bracket and RegenCy Plus Bracket, designed for dental alignment treatments.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Regency Bracket Ref K936244
Regimes: 510(k) Registry: 510(k)Regency Plus Bracket Ref K933758
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mid-American Dental Specialties, Inc. have in the registry?
The registry currently lists 2 devices for Mid-American Dental Specialties, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mid-American Dental Specialties, Inc.'s devices?
Among its 2 most recently registered devices, Mid-American Dental Specialties, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mid-American Dental Specialties, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mid-American Dental Specialties, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mid-American Dental Specialties, Inc. in the registry?
The most recently registered devices listed for Mid-American Dental Specialties, Inc. include REGENCY BRACKET and REGENCY PLUS BRACKET.