Technology Marketing Group
Country not established
- Devices
- 3
What Technology Marketing Group makes
The company manufactures ultrathin flexible endoscopes, including models like the TAS-211/2.3 and variants under the TAS series, designed for minimally invasive diagnostic and procedural applications.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Tas-211/2.3 Ultrathin Flexible Endoscope Ref K935834
Regimes: 510(k) Registry: 510(k)Ultathin Flexible Endoscope Ref K941715
Regimes: 510(k) Registry: 510(k)Tas-(Various) Ultrathin Flexible Endoscope Ref K942388
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technology Marketing Group have in the registry?
The registry currently lists 3 devices for Technology Marketing Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technology Marketing Group's devices?
Among its 3 most recently registered devices, Technology Marketing Group has devices listed in FDA 510(k) (3 devices).
What risk classes do Technology Marketing Group's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Technology Marketing Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technology Marketing Group in the registry?
The most recently registered devices listed for Technology Marketing Group include TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE, ULTATHIN FLEXIBLE ENDOSCOPE and TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE.