Trident Dental, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Trident Dental, Inc. makes
Trident Dental, Inc. manufactures dental mouth props, including models named ROYAL and WINDSOR, designed for patient positioning and oral access during procedures. These devices are intended for use in clinical settings to maintain proper mouth alignment and improve operator access during dental treatments.
The company’s products fall under FDA Class II devices and are authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Royal Ref K800866
510(k) 510(k)Windsor Ref K800865
510(k) 510(k)Dental Mouth Prop. Ref K802696
510(k) 510(k)
Frequently asked questions
How many devices does Trident Dental, Inc. have in the registry?
The registry currently lists 3 devices for Trident Dental, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trident Dental, Inc.'s devices?
Among its 3 most recently registered devices, Trident Dental, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Trident Dental, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Trident Dental, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trident Dental, Inc. in the registry?
The most recently registered devices listed for Trident Dental, Inc. include ROYAL, WINDSOR and DENTAL MOUTH PROP..