Neobiotech Co., Ltd.
FDA 510(k) medical device clearances.
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.