U&I Corporation
U&I Corporation holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2022.
Top product codes for U&I Corporation
Recent clearances by U&I Corporation
- K220147 — Aspiron S ACP System
- K210573 — Velofix SA Cervical Cage
- K183243 — Velofix TLIF Cage
- K190067 — Velofix Interbody Fusion System
- K190053 — SECULOK ACP System
- K181824 — CBT Screw Fixation System
- K183383 — ANAX OCT Spinal System
- K181829 — Velofix TLIF Cage
- K182055 — SECULOK ACP System
- K180759 — SECULOK Suture Anchor
- K173198 — Facet Screw Fixation System
- K173524 — ANAX 5.5 Spinal System
- K172419 — Velofix TLIF Cage
- K172424 — Velofix SA Cervical Cage
- K171749 — Velofix(tm) Interbody Fusion System
- K162189 — ANAX 5.5 Spinal System
- K143631 — Benefix Interspinous Fixation System
- K150570 — ANAX OCT Spinal System
- K143417 — ANAX 5.5 Spinal System
- K132797 — L'DISQ
- K132218 — PERFIX ILIAC SCREW SYSTEM
- K132101 — ANAX 5.5 SPINAL SYSTEM
- K131200 — ASPIRON ACP SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.