Rochester Electro-Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 212
What Rochester Electro-Medical, Inc. makes
Rochester Electro-Medical, Inc. manufactures disposable pre-gelled surface electrodes for medical monitoring and ultrastructural concentric needles designed for precision medical procedures.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company operates within the United States.
Catalogue
Search and filter all 212 devicesShowing 1-50 of 212
Company details
- DUNS number
- 068156330
- [email protected]
- Phone
- 18003285544
Frequently asked questions
How many devices does ROCHESTER ELECTRO-MEDICAL, INC. have in the registry?
The registry currently lists 212 devices for ROCHESTER ELECTRO-MEDICAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ROCHESTER ELECTRO-MEDICAL, INC.'s devices?
Among its 50 most recently registered devices, ROCHESTER ELECTRO-MEDICAL, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do ROCHESTER ELECTRO-MEDICAL, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for ROCHESTER ELECTRO-MEDICAL, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ROCHESTER ELECTRO-MEDICAL, INC. in the registry?
The most recently registered devices listed for ROCHESTER ELECTRO-MEDICAL, INC. include EverLast™ BMS037T15-4, Horizon™ S91690-50/PK, Horizon™ S86025-T1 and EverLast™ MS615015.