Ldr Spine USA, Inc.
Ldr Spine USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2017, with 1 FDA device recall on record.
Top product codes for Ldr Spine USA, Inc.
FDA recalls by Ldr Spine USA, 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 Ldr Spine USA, Inc.
- K162133 — VerteFIT Corpectomy Cage System
- K161173 — Avenue® T TLIF Cage
- K161798 — FacetBRIDGE® System
- K142645 — Avenue T TLIF Cage
- K133363 — INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
- K123134 — EASYSPINE SYSTEM
- K121103 — LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S
- K113285 — LDR SPINE USA AVENUE L INTERBODY FUSION
- K120760 — LDR SPINE SPINETUNE TL SPINAL SYSTEM
- K113559 — LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.