Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Zimmer BiometLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Lanx with 36 510(k) clearances and 1 device recall. The most recent is a device recall dated Nov 4, 2013: LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split Tip Driver - Sh….
| Nov 4, 2013 | LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split Tip Driver - Short ("Driver"). Model Number 8630-0107. The TimbeClass II · Lanx, Inc. is recalling various lots of Timberline MPF Straight Split Tip Driver - Short ("Driver") because the width of | Device recalls |
| Jul 12, 2013 | LANX FUSION SYSTEMK131547 · OVD | 510(k) clearances |
| May 24, 2013 | LANX SPINAL FIXATION SYSTEMK131156 · KWP | 510(k) clearances |
| Mar 18, 2013 | LANX FUSION SYSTEM- SAK123767 · OVD | 510(k) clearances |
| Sep 10, 2012 | LANX SPINAL FIZATION SYSTEMK121316 · NKB | 510(k) clearances |
| Aug 17, 2012 | LANX SPINAL FIXATION SYSTEMK122145 · NKB | 510(k) clearances |
| Aug 2, 2012 | LANX SPINAL FIXATION SYSTEMK121940 · NKB | 510(k) clearances |
| Mar 9, 2012 | LANX SPINAL FIXATION SYSTEMK120399 · NKB | 510(k) clearances |
| Dec 19, 2011 | LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)K113434 · NKB | 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
