Her-Mar, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Her-Mar, Inc. makes
Her-Mar, Inc. manufactures electronic clinical thermometers designed for precise body temperature measurement in healthcare settings, as well as disposable surgical instruments for single-use procedures.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Thermometer, Electronic Clinical Ref K810814
Regimes: 510(k) Registry: 510(k)Surgical Instrument, Disposable Ref K940684
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Her-Mar, Inc. have in the registry?
The registry currently lists 2 devices for Her-Mar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Her-Mar, Inc.'s devices?
Among its 2 most recently registered devices, Her-Mar, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Her-Mar, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Her-Mar, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Her-Mar, Inc. in the registry?
The most recently registered devices listed for Her-Mar, Inc. include THERMOMETER, ELECTRONIC CLINICAL and SURGICAL INSTRUMENT, DISPOSABLE.