31 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
Suture, Nonabsorbable, Synthetic, Polyester
FDA Pre-Market Approval
FDA Class 2
·NON-ABSORBABLE (POLYESTER FIBER) SUTURES
N/A
FDA UDI
GEORGE TIEMANN & CO.·B582083509·RETRACTOR, ALL TYPES
Optetrak Logic
FDA UDI
Exactech, Inc.·10885862159281·
Optetrak Logic
FDA UDI
Exactech, Inc.·10885862241122·TRIAL, CR TIBIAL INSERT, LOGIC®, SIZE 3.5, 9mm,...
Truliant
FDA UDI
Exactech, Inc.·10885862306852·
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 9, 2025
TRULIANT CR CEM FEM CR CEM LEFT SZ 3.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 16, 2025
LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 26, 2026
LOGIC CR TIBIAL INSERT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 26, 2026
LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 21, 2024
FINELINE
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code DTB·February 8, 2002