Ultramed, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Ultramed, Inc. makes
Ultramed, Inc. manufactures ultrasound-based medical imaging and surgical systems, including vascular imaging and Doppler systems for assessing blood flow, transcranial Doppler devices for cerebral circulation monitoring, and phacoemulsification tools for cataract surgery. Their portfolio includes ultrasonic fragmentation systems and phacoemulsification tips designed for ophthalmic procedures.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database. Ultramed, Inc. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Transcran(Tm) Transcranial Pulsed Doppler System Ref K882015
Regimes: 510(k) Registry: 510(k)Phacoemulsification Ultrasonic Fragment System Ref K862021
Regimes: 510(k) Registry: 510(k)Phacoemulsification Tip Ref K850578
Regimes: 510(k) Registry: 510(k)Dopplex Ultrasonic Doppler System Ref K873989
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultramed, Inc. have in the registry?
The registry currently lists 5 devices for Ultramed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultramed, Inc.'s devices?
Among its 5 most recently registered devices, Ultramed, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Ultramed, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Ultramed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultramed, Inc. in the registry?
The most recently registered devices listed for Ultramed, Inc. include ULTRAMED TF 122 ULTRASON VASCU IMAG & DOPPLER SYST, TRANSCRAN(TM) TRANSCRANIAL PULSED DOPPLER SYSTEM, PHACOEMULSIFICATION ULTRASONIC FRAGMENT SYSTEM and PHACOEMULSIFICATION TIP.