Ceterix Orthopedics, Inc.

FDA Regulatory Profile

Ceterix Orthopedics, Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2945-2018, Class II) was initiated on May 16, 2018.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2945-2018Class IICeterix Disposable Knot Pusher / Suture Cutter; NovoCut Suture Manager. Model# CTX-C001. orthopedicMay 16, 2018
Z-0250-2016Class IINovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended forOctober 13, 2015