Terraflex
IsraelFDA applicant, unverified
- Devices
- 1
What Terraflex makes
Terraflex manufactures single-use dental tools, including the DentFlex Disposable Dental Saliva Ejector, designed for oral hygiene procedures in clinical settings.
The company’s portfolio is regulated under FDA Class I devices and appears in the FDA 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Dentflex Displosable Dental Saliva Ejector Ref K940769
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Terraflex have in the registry?
The registry currently lists 1 device for Terraflex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Terraflex's devices?
Among its 1 most recently registered device, Terraflex has devices listed in FDA 510(k) (1 device).
What risk classes do Terraflex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Terraflex's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Terraflex in the registry?
The most recently registered devices listed for Terraflex include DENTFLEX DISPLOSABLE DENTAL SALIVA EJECTOR.