Osteogenics Biomedical, Inc.

8 FDA 510(k) medical device clearances.

Top product codes for Osteogenics Biomedical, Inc.

NBY — General, Plastic Surgery 2 devices
NPK — Dental 2 devices
DZL — Dental 1 device
JEY — Dental 1 device
KKY — General, Plastic Surgery 1 device
LYC — Dental 1 device

Recent clearances by Osteogenics Biomedical, Inc.

K201187 — Cytoplast Titanium-Reinforced PTFE Membranes NPK · 2021-01-23
K171774 — RPM Reinforced PTFE Mesh NPK · 2017-10-19
K093719 — PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT# DZL · 2010-03-01
K072076 — CYTOPLAST PTFE SUTURE NBY · 2007-10-31
K013764 — IMMIX BONE GRAFT EXTENDER KKY · 2002-05-16
K003028 — CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC NBY · 2000-11-24
K993610 — CYTOPLAST RESORB, MODELS R-250, RP-250, RU-250, RPS-250, RPL-250 LYC · 2000-03-02
K984230 — OSTEO-MESH TM-300 JEY · 1999-02-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.