17 results · 22ms · Sources: EU EUDAMED, US FDA

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Suture, Nonabsorbable, Synthetic, Polyester

FDA Pre-Market Approval
FDA Class 2 ·DACRON SURGICAL SUTURES

DESS dental smart solutions

FDA UDI
TERRATS MEDICAL SL.·08435457209959·Internal Hex "Click"

VAN-TEC ENDOPYELOTOMY KNIFE

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·N-18 (KOLFOCON A),N-32 (KOLFOCON B) LENS MATERIAL

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·EPCON SOFT (POLYMACON) SPHERICAL AND TORIC LENSES

Lens, Contact (Other Material) - Daily

FDA Pre-Market Approval
FDA Class 2 ·N-18 (KOLFOCON A),N-32 (KOLFOCON B) LENS MATERIAL

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·EPCON SOFT (POLYMACON) SPHERICAL AND TORIC LENSES

SILICONE ULTRAVIOLET ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 8, 2006

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FDA Adverse Event
Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006

SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Injury ·STAAR SURGICAL COMPANY·Product code HQL·June 26, 2006

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 22, 2010

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 31, 2014

ASR UNI FEMORAL IMPL SIZE 46

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·December 19, 2012

SEE H-10

FDA Adverse Event
Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·October 10, 2012

SEE H-10

FDA Adverse Event
Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·March 27, 2012