Sonicaid, Inc.
United StatesFDA applicant, unverified
- Devices
- 18
What Sonicaid, Inc. makes
Sonicaid, Inc. manufactures fetal monitoring systems, including handheld fetal heart detectors and continuous monitoring devices like the FM3R and FM5 models. The company also produces vascular imaging tools such as the Vasoview duplex imaging system and Vasopulse Model 5000 for blood flow assessment. Additional products include vascular flow detectors (BV105 series), impedance plethysmography systems (Vasoscreen), and mini-monitors like the AP 180. Transducer accessories, such as the 5 MHz transducer, complement these diagnostic devices.
These devices are classified under FDA regulations as Class I and Class II medical devices, with some models requiring 510(k) clearance. The portfolio is listed in the FDA’s 510(k) registry, reflecting their regulatory status. The company is headquartered in the United States.
Catalogue
Search and filter all 18 devicesFrequently asked questions
How many devices does Sonicaid, Inc. have in the registry?
The registry currently lists 18 devices for Sonicaid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonicaid, Inc.'s devices?
Among its 18 most recently registered devices, Sonicaid, Inc. has devices listed in FDA 510(k) (18 devices).
What risk classes do Sonicaid, Inc.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for Sonicaid, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonicaid, Inc. in the registry?
The most recently registered devices listed for Sonicaid, Inc. include FETAL HEART DETECTOR #D206, FETAL MONITORING SYS. MODEL FM3R, SONICOMP and VASOVIEW DUPLEX IMAGING SYSTEM.