Turtlebrace
Active in EUDAMEDCanadafrom SRN EUDAMED FDA SRN CA-MF-000055922 FEI 3017434835
- Devices
- 59
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What Turtlebrace makes
Turtlebrace manufactures the Turtlebrace Thumb Add-On, a Class I medical device designed to provide support and stabilization for the thumb.
The device is regulated as a Class I product and is listed in the Eudamed registry. Turtlebrace is based in Canada.
Catalogue
Search and filter all 59 devicesShowing 1-50 of 59
Company details
- EUDAMED SRN
- CA-MF-000055922
- FDA FEI number
- 3017434835
- EUDAMED status
- Active
- EUDAMED registered name
- Turtlebrace
- Registered address
- 3100, Boulevard Choquette, QC J2S 1H1, St-Hyacinthe, Canada
- [email protected]
- PRRC contact
- Serge-Eric Blais
Frequently asked questions
How many devices does Turtlebrace have in the registry?
The registry currently lists 59 devices for Turtlebrace. Devices recorded under merged duplicate company entries are counted once.
Which registries list Turtlebrace's devices?
Among its 50 most recently registered devices, Turtlebrace has devices listed in EUDAMED (50 devices).
What risk classes do Turtlebrace's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Turtlebrace's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Turtlebrace in the registry?
The most recently registered devices listed for Turtlebrace include Turtlebrace Ankle Brace, Pediatric, Standard, Medium, Turtlebrace Wrist Brace, Infant, Zipper, Medium, Turtlebrace Ankle Brace, Pediatric, Standard, Large and Turtlebrace Wrist Brace, Infant, Hook and Loop, Small.