Spinalight, Inc.
Spinalight, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 4 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on Jun 20, 2018.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 4
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K172536 | Atlas Percussion Adjusting Instrument | Jun 20, 2018 |
| K001476 | TORQUE INSTRUMENT, MODEL 8500 | Aug 4, 2000 |
| K955540 | HAND HELD ATLAS INSTRUMENT | Mar 4, 1996 |
| K946258 | MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENT | Nov 20, 1995 |
| K945954 | MODELS 4100 AND 4300 MULTITHERAPY | Jan 19, 1995 |
| K933621 | HILO TABLE | Jan 7, 1994 |
| K933622 | FLEXION DISTRACTION TABLE | Jan 7, 1994 |