56 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Psoria-Shield AURORA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Futar
FDA UDI
Kettenbach GmbH & Co. KG·E2171192411·Futar Easy Fast Normal pack
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019101·2.4mm x 11mm Cannulated Lag Screw
Symetri Clear
FDA UDI
ORMCO CORPORATION·00889989083064·L3L SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVISI...
32MM MOD HEAD COCR -3MM NECK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·July 21, 2017
ARCOMXL 32MM +3 MROM LNR SZ 22
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LZO·July 14, 2017
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690198666·AK3 Ultra Insert Trial Size 4, 11mm
ARCOM XL RINGLOC ACETABULAR LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·December 15, 2016
ARCOM XL RINGLOC ACETABULAR LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LZO·May 9, 2017
MODULAR HEAD COMPONENT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·May 9, 2017
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070607·Cannulated 2.4 x 11mm Lag Screw Sterile Qty 5
MAMMOTOME ELITE BIOPSY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PEARLESCENT POWDER FREE NITRILE EXAMINATION GLOVES WITH ALOE VERA (YELLOW, RED, GREEN, BLACK, BLUE)
FDA 510(k)
FDA Class 1
·General Hospital
E1 RINGLOC ACETABULAR LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·June 20, 2017
GORE TAG THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 7, 2008
*
FDA Adverse Event
Malfunction
·WESCOR, INC.·Product code KTB·August 1, 2011
2.7MM TI VA LCKNG SCR SLF-TPNGWITH T8 STARDRIVE RECESS 26MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·June 27, 2013
MALLORY/HEAD RADIAL SHELL POROUS COAT 58MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LZO·May 3, 2017
M2A-MAGNUM 52-60MM TPR INSRT-3
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·March 23, 2022
FREEDOM CONSTRAINED MODULAR HEAD STANDARD NECK 36MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWZ·May 3, 2017