Surgical Appliance Industries, Inc. is one of 14462 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Appliance Industries, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLET
9
Total
9
Cleared
0
Denied
Surgical Appliance Industries, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1981 to 2012. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Surgical Appliance Industries, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Surgical Appliance Industries, Inc.
9 devices
Cleared
Apr 27, 2012
TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR...
General Hospital
15d
Cleared
Jun 24, 1982
TRUNCAL ORTHOSIS
Physical Medicine
16d
Cleared
Jan 18, 1982
EXTERNAL BREAST PROSTHESIS
General & Plastic Surgery
42d
Cleared
Sep 14, 1981
CRUCIFORM ANTERIOR SPINAL HYPEREXTEN. O
Physical Medicine
25d
Cleared
Sep 14, 1981
CUSTOM CONTOUR LUMBOSACRAL ORTHOSIS
Physical Medicine
21d
Cleared
Sep 14, 1981
NEOPRENE KNEE SUPPORT
Physical Medicine
21d
Cleared
Jun 25, 1981
CYLINDER KNEE CAST/SPLINT
Physical Medicine
10d
Cleared
Jun 25, 1981
ANKLE-FOOT CAST/SPLINT
Physical Medicine
10d
Cleared
Jun 16, 1981
LUMBO-SACRAL FLEXION ORTHOSIS
Physical Medicine
20d