Surgical Appliance Industries, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K121106 | TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLET | April 27, 2012 |
| K821682 | TRUNCAL ORTHOSIS | June 24, 1982 |
| K813416 | EXTERNAL BREAST PROSTHESIS | January 18, 1982 |
| K812401 | CRUCIFORM ANTERIOR SPINAL HYPEREXTEN. O | September 14, 1981 |
| K812422 | CUSTOM CONTOUR LUMBOSACRAL ORTHOSIS | September 14, 1981 |
| K812423 | NEOPRENE KNEE SUPPORT | September 14, 1981 |
| K811690 | ANKLE-FOOT CAST/SPLINT | June 25, 1981 |
| K811689 | CYLINDER KNEE CAST/SPLINT | June 25, 1981 |
| K811494 | LUMBO-SACRAL FLEXION ORTHOSIS | June 16, 1981 |