12 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMR Lateralized Connectors with screws
FDA 510(k)
FDA Class 2
·Orthopedic
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304270589·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515135543·Chung Weitlaner Retractor, 4 1/2", Blunt Tips, ...
ATMOS E 201 THORAX AND ATMOS S 201 THORAX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
WOUND FLUSH, STERILE WATER & NORMAL SALINE
FDA 510(k)
FDA Unclassified
·Unknown
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/11 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·June 5, 2024
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY AG·Product code MTA·October 17, 2014
CONTOUR CURVED CUTTER STAPLER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 28, 2011
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 21, 2013
CHROMID STREPTO B AGAR
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code PQZ·November 1, 2017
CHROMID STREPTO B AGAR
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code PQZ·November 1, 2017
Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous retrieval of cardiac leads. Order Number (GPN): G20003 Reference Part Number (RPN): LR-CLP001
FDA Enforcement
Class II
·Ongoing·Cook Vandergrift, Inc.·September 13, 2023