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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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High-speed Turbine Handpieces for Single Use
FDA UDI
Beijing Dongbo Dental Handpiece Co.,Ltd.·06970278690279·
ANK IMPL B11 D4,5 MM/L11 MM
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZG·June 28, 2022
GLYCOLON
FDA Adverse Event
Malfunction
·RESORBA MEDICAL GMBH·Product code DZG·July 13, 2023
GLYCOLON
FDA Adverse Event
Malfunction
·RESORBA MEDICAL GMBH·Product code DZG·July 13, 2023
REPLACE SELECT TAPERED TIU RP 4.3X13MM
FDA Adverse Event
Injury
·NOBEL BIOCARE AB·Product code DZG·December 21, 2005
ROTATING SURGICAL PUNCH - FLAT TIP
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code DZG·August 2, 2022
SCREW-VENT DENTAL IMPLANT
FDA Adverse Event
Injury
·CORE-VENT BIO-ENGINEERING·Product code DZG·July 13, 1995
UNKNOWN ATIS ABUTMENT
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZG·November 9, 2022
Suture, Dental
FDA classification
FDA Class 3
·Suture, Dental
DRG International, Inc.
FDA registration
DRG International, Inc.·94 products·🇺🇸 United States
DRG INSTRUMENTS GMBH
FDA registration
DRG INSTRUMENTS GMBH·95 products·🇩🇪 Germany
DMG America LLC
FDA registration
DMG America LLC·11 products·🇺🇸 United States
High-speed Turbine Handpieces for Single Use
FDA UDI
Beijing Dongbo Dental Handpiece Co.,Ltd.·06970278690330·
ALLEVA MEDICAL (D.G.) LTD
FDA registration
ALLEVA MEDICAL (D.G.) LTD·13 products·🇨🇳 China
DMG DIGITAL ENTERPRISES SE
FDA registration
DMG DIGITAL ENTERPRISES SE·7 products·🇩🇪 Germany
DCG DATA TERMINAL
FDA 510(k)DCG-VII ELECTROCARDIOSCANNER
FDA 510(k)
FDA Class 2
·Cardiovascular
DCG PREAMPLIFIER MODULE
FDA 510(k)
FDA Class 2
·Cardiovascular
DMG CHEMISCH PHARMAZEUTISCHE FABRIK GMBH
FDA registration
DMG CHEMISCH PHARMAZEUTISCHE FABRIK GMBH·19 products·🇩🇪 Germany
THYMINE/THYMIDINE DISCS DDG
FDA 510(k)
FDA Class 1
·Microbiology