Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Spinalight with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 20, 2018: Atlas Percussion Adjusting Instrument.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 20, 2018 | Atlas Percussion Adjusting InstrumentK172536 · LXM | 510(k) clearances |
| Aug 4, 2000 | TORQUE INSTRUMENT, MODEL 8500K001476 · LXM | 510(k) clearances |
| Mar 4, 1996 | HAND HELD ATLAS INSTRUMENTK955540 · LXM | 510(k) clearances |
| Nov 20, 1995 | MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENTK946258 · LXM | 510(k) clearances |
| Jan 19, 1995 | MODELS 4100 AND 4300 MULTITHERAPYK945954 · JFB | 510(k) clearances |
| Jan 7, 1994 | HILO TABLEK933621 · INQ | 510(k) clearances |
| Jan 7, 1994 | FLEXION DISTRACTION TABLEK933622 · INQ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
