Lanx, Inc.
Lanx, Inc. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2013, with 1 FDA device recall on record.
Top product codes for Lanx, Inc.
FDA recalls by Lanx, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Lanx, Inc.
- K131547 — LANX FUSION SYSTEM
- K131156 — LANX SPINAL FIXATION SYSTEM
- K123767 — LANX FUSION SYSTEM- SA
- K121316 — LANX SPINAL FIZATION SYSTEM
- K122145 — LANX SPINAL FIXATION SYSTEM
- K121940 — LANX SPINAL FIXATION SYSTEM
- K113434 — LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
- K112388 — LANX CERVICAL SA
- K103091 — LANX SPINAL FIXATION SYSTEM
- K103237 — LANX SPINAL SYSTEM
- K103666 — LANX LATERAL
- K103660 — LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
- K100888 — MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM
- K101364 — LANX FACET SCREW SYSTEM
- K100935 — LANX SPINAL FIXATION SYSTEM
- K100191 — LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
- K092765 — LANX ANTERIOR PLATING SYSTEM
- K092656 — LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM
- K092536 — SPINAL FIXATION SYSTEM
- K083815 — LANX FUSION SYSTEM
- K083581 — LANX SPINAL FIXATION SYSTEM
- K090316 — MODIFICATION TO: LANX ANTERIOR CERVICAL PLATE SYSTEM
- K090252 — MODIFICATION TO: LANX SPINAL FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.