Ulrich GmbH & Co. KG
Ulrich GmbH & Co. KG holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2025.
Top product codes for Ulrich GmbH & Co. KG
Recent clearances by Ulrich GmbH & Co. KG
- K252281 — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
- K251295 — ulrichINJECT CT Motion (XD 8000)
- K241850 — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
- K233737 — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
- K210541 — ulrichINJECT CT motion
- K202227 — Artus cervical plate system
- K192872 — ulrichINJECT CT Motion
- K192117 — Small VBR
- K171392 — ulrichINJECT CT motion
- K161032 — neon3 universal OCT spinal stabilization
- K161723 — ulrich Transfer Set
- K150650 — neon3
- K122957 — TEZO TITANIUM CAGE FAMILY
- K123717 — UCENTUM
- K120891 — TANGORS MULTIFUNCTIONAL POSTERIOR SYSTEM
- K113346 — NEON SYSTEM
- K103814 — PEZO INTERBODY CAGES SYSTEM
- K101353 — GOLDEN GATE ANTERIOR PLATE SYSTEM
- K102853 — FLAMENCO SPINAL FIXATION SYSTEM
- K090861 — MAMBO, MODEL CS 18XX-XX
- K090841 — ADDPLUS
- K080841 — COSMIC SYSTEM
- K060416 — OBELISC VERTEBRAL BODY REPLACEMENT DEVICE
- K052385 — TANGORS POLYAXIAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.