Company ยท US
Spinalight, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2018. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 20, 2018 | K172536 | Atlas Percussion Adjusting Instrument Spinalight, Inc. | LXM |
| Aug 4, 2000 | K001476 | TORQUE INSTRUMENT, MODEL 8500 Spinalight, Inc. | LXM |
| Mar 4, 1996 | K955540 | HAND HELD ATLAS INSTRUMENT Spinalight, Inc. | LXM |
| Nov 20, 1995 | K946258 | MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENT Spinalight, Inc. | LXM |
| Jan 19, 1995 | K945954 | MODELS 4100 AND 4300 MULTITHERAPY Spinalight, Inc. | JFB |
| Jan 7, 1994 | K933622 | FLEXION DISTRACTION TABLE Spinalight, Inc. | INQ |
| Jan 7, 1994 | K933621 | HILO TABLE Spinalight, Inc. | INQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||