Medtrex, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Electrosurgical Dispersive Electrode Ref K952577
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtrex, Inc. have in the registry?
The registry currently lists 4 devices for Medtrex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtrex, Inc.'s devices?
Among its 4 most recently registered devices, Medtrex, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medtrex, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medtrex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtrex, Inc. in the registry?
The most recently registered devices listed for Medtrex, Inc. include HYDROCOOL DUAL CONDUCTOR POLYMER GEL (30101-001/CORDED DISPERSIVE ELECTRODE-SENSING, ENCORE ELECTROSURGICAL HANDCONTROL PENCIL (35001-001), ELECTROSURGICAL DISPERSIVE ELECTRODE and O.R.PRO 300 ELECTROSURGICAL GENERATOR MODEL 40001-100.