Bahadir Sterilization Containers

510(k) Number

K233578 ↗

FDA product code

KCT

FDA applicant

Bahadir USA, LLC

Device class

Class II

Regulation

21 CFR Part 880.6850

Advisory committee

General Hospital

FDA decision

SESE Substantially Equivalent

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Other devices filed under FDA product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories).

• Surgical and Prosthetic Trays by DENTSPLY SIRONA INC
• STERILEDGE SELF SEAL POUCH by Beacon Converters, Inc.
• ERMIS ER190.070 by Ermis MedTech GmbH
• Neodent Implant System - Helix Short Surgical Kit Cases by JJGC Indústria e Comércio de Materiais Dentários S/A.
• SterilContainer S2 System by AESCULAP, INC.
• SURGICAL INSTRUMENT TMECC 03 by S.I.N. - Sistema DE Implante Nacional S.A.
• Jewel Precision Reusable Rigid Sterilization Container System by Jewel Precision Sheet Metal & Machine, Inc.
• SURGICAL INSTRUMENT KRFT by S.I.N. - Sistema DE Implante Nacional S.A.
• OsteoMed QuickFix Hybrid MMF Sterilization Tray by Osteomed Corp.
• Biotech Dental Kits by BIOTECH DENTAL

• Bahadir USA Y100.97M

  Class II

  FDA 510(k) K131407 Active Cleared 12 Aug 2014 GUDID on market

• Bahadir USA Y105.92M

  Class II

  FDA 510(k) K131407 Active Cleared 12 Aug 2014 GUDID on market

• Bahadir USA Y106.92M

  Class II

  FDA 510(k) K131407 Active Cleared 12 Aug 2014 GUDID on market

• Bahadir USA Y110.92M

  Class II

  FDA 510(k) K131407 Active Cleared 12 Aug 2014 GUDID on market

See all devices from Bahadir USA LLC →