13 results · 24ms · Sources: EU EUDAMED, US FDA

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AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112571·BARRON CORNEAL PUNCH 6.5MM

LACTOSORB L15 SCREW ANCHOR WITH LACTOCARBONATE SUTURE

FDA 510(k)
FDA Class 2 ·Orthopedic

TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRI PRO PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 21, 2025

3CC-E CMB 25X 5/8 A

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FMI·November 7, 2008

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·September 1, 2011

REFLEX-HYBRID 1 LEVEL ACP SIZE 16MM

FDA Adverse Event
Malfunction ·STRYKER SPINE-FRANCE·Product code KWQ·July 17, 2013

ANN PH NAIL RT 9X160MM

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code HSB·July 24, 2025

ANN BLUNT TIP SCREW 4X54MM

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code HSB·July 24, 2025

ANN BLUNT TIP SCREW 4X50MM

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code HSB·July 24, 2025

ANN BLUNT TIP SCREW 4X48MM

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code HSB·July 24, 2025

Posey Connecting Strap/Belt, Cotton, 72" (232072). Intended for medical purposes to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others.

FDA Recall
Terminated ·J T Posey Company·Product code FMQ·April 20, 2009