Neobiotech Co., Ltd.
Neobiotech Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2024.
Top product codes for Neobiotech Co., Ltd.
Recent clearances by Neobiotech Co., Ltd.
- K232528 — Protective Cap
- K232049 — IS-III active Short Implant
- K210903 — IS Multi Unit Abutment System
- K190849 — IS-III active System_S-narrow Type
- K181137 — IT-III active System
- K181138 — IS-III active System
- K181178 — S-mini active Fixture
- K173938 — IS-III HActive Fixture
- K160991 — Neo GBR System
- K120503 — CMI IMPLANT IS II ACTIVE
- K113554 — CMI IMPLANT IS SYSTEM
- K112540 — S-MINI IMPLANT SYSTEM
- K111761 — NEO TITANIUM MESH, CTI-MEM
- K090377 — SINUS QUICK EB SYSTEM
- K090825 — SQ IS SYSTEM
- K090527 — SINUS QUICK IT SYSTEM
- K042339 — NEOPLANT IMPLANT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.