The Silcraft Corp. is one of 7141 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Silcraft Corp. - FDA 510(k) Cleared Devices
Recent clearances: XTANK2 MOBILE EXTREMITY WHIRLPOOL SYSTEM, SILCRAFT ACCESS 3700 WHIRLPOOL SYSTEM, SILCRAFT MODEL 1800 LIFT, SILCRAFT DISINFECTANT
2
Total
2
Cleared
0
Denied
The Silcraft Corp. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 1998 to 1998. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by The Silcraft Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Silcraft Corp.
2 devices