Cowellmedi Co., Ltd.
Cowellmedi Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2025.
Top product codes for Cowellmedi Co., Ltd.
Recent clearances by Cowellmedi Co., Ltd.
- K242287 — SFIT Abutment
- K241127 — INNO SLA Mini Plus® Implant System
- K231411 — INNO SLA Submerged Hybrid Ti-Base System
- K232546 — Meta G UCLA Abutment
- K231395 — INNO SLA Submerged Narrow Implant System
- K211554 — InnoGenic Non-resorbable Membrane
- K201323 — INNO SLA Submerged Implant System
- K132242 — INNO SLA SUBMERGED IMPLANT SYSTEM
- K100850 — COWELL IMPLANT SYSTEM
- K090054 — ATLAS IMPLANT SYSTEM - WIDE PLUS
- K090049 — ATLAS IMPLANT SYSTEM- MINI PLUS
- K071148 — ATLAS IMPLANT SYSTEM
- K050635 — ALLFIM IMPLANT SYSTEMS
- K041655 — BIO PLANT SYSTEM (IMPLANTS AND ABUTMENTS)
Data sourced from openFDA. This site is unofficial and independent of the FDA.