The Medtech Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What The Medtech Group, Inc. makes
The Medtech Group, Inc. manufactures the EN-TRAP syringe, a specialized medical syringe designed for controlled drug delivery or fluid extraction, and the Medtech C.P.R. mask, a resuscitation device used to provide oxygen and ventilation during cardiopulmonary resuscitation.
The company’s products are regulated under FDA Class I and Class II classifications, with the EN-TRAP syringe and Medtech C.P.R. mask listed via the 510(k) pathway. These devices are registered in the FDA’s 510(k) database. The company is headquartered in the United States.
Catalogue
En-Trap Syringe Ref K895203
Regimes: 510(k) Registry: 510(k)Medtech C.P.R. Mask Ref K862199
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Medtech Group, Inc. have in the registry?
The registry currently lists 2 devices for The Medtech Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Medtech Group, Inc.'s devices?
Among its 2 most recently registered devices, The Medtech Group, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do The Medtech Group, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Medtech Group, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Medtech Group, Inc. in the registry?
The most recently registered devices listed for The Medtech Group, Inc. include EN-TRAP SYRINGE and MEDTECH C.P.R. MASK.