Sonics & Materials, Inc. is one of 7883 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonics & Materials, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VIBRA-SURGE SYSTEM MODEL VS2120
1
Total
1
Cleared
0
Denied
Sonics & Materials, Inc. is a leader in ultrasonic technology with a manufacturing facility in Danbury, Connecticut. Founded in 1969, the company specializes in ultrasonic liquid processing and welding systems. The company has over 55 years of experience delivering precision equipment across hundreds of industries worldwide.
Sonics & Materials received 1 FDA 510(k) clearance from 1 total submission. The cleared device falls under General & Plastic Surgery devices. The company's regulatory clearance dates to 1997. The company is currently inactive, with no new FDA submissions or clearances in more than five years, and should be treated as a historical regulatory record.
The cleared device, the VIBRA-SURGE SYSTEM MODEL VS2120, represents the company's work in surgical and medical applications. Sonics' broader product portfolio includes ultrasonic processors for laboratory and production scales, ultrasonic welding systems for plastics and metals, and ultrasonic cutting equipment. The company maintains ISO 9001:2015 certification and emphasizes technical support and applications expertise.
Explore the company's FDA 510(k) clearance history, device names, and regulatory milestones in the database records below.
FDA 510(k) Regulatory Record - Sonics & Materials, Inc.
1 devices