Huntleigh Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 23
What Huntleigh Technology, Inc. makes
Huntleigh Technology, Inc. manufactures medical devices for patient monitoring, fetal assessment, and critical care support, including dynamic flotation systems for patient positioning, alternating pressure mattresses, and air-hand garments for pressure injury prevention. Their portfolio includes Doppler ultrasound devices for fetal and vascular monitoring, such as the Multi Dopplex and Rheo Dopplex II, as well as air pumps and traction machines for therapeutic applications. The company also produces antepartum fetal monitors and portable pressure garments for limb or joint support.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance obtained through the 510(k) pathway. Products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 23 devicesFrequently asked questions
How many devices does Huntleigh Technology, Inc. have in the registry?
The registry currently lists 23 devices for Huntleigh Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Huntleigh Technology, Inc.'s devices?
Among its 23 most recently registered devices, Huntleigh Technology, Inc. has devices listed in FDA 510(k) (23 devices).
What risk classes do Huntleigh Technology, Inc.'s devices fall under?
Among its 23 most recently registered devices, the classes recorded for Huntleigh Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Huntleigh Technology, Inc. in the registry?
The most recently registered devices listed for Huntleigh Technology, Inc. include HUNTLEIGH DYNAMIC FLOTATION SYSTEM, HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5, DOPCORD PPG and MULTI DOPPLEX, MD-1.