21 results · 23ms · Sources: EU EUDAMED, US FDA

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FLASH PENTA MB QUICK, FLASH MB QUICK

FDA 510(k)
FDA Class 2 ·Dental

VELNEZ

FDA UDI
DATT MEDIPRODUCTS PRIVATE LIMITED·08904340408248·VELNEZ Nasal Pack 6 cm x 2 cm

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017781·K-Wire, Double Ended, Trocar Point, Diameter Si...

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481120923·LOCATOR R-Tx Abutment For UF(II) Regular/Wide I...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017798·K-Wire, Double Ended, Trocar Point, Diameter 0....

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319740828·Foerster Sponge (Ring) Forceps 9-1/2" (23.8cm),...

VELNEZ

FDA UDI
DATT MEDIPRODUCTS PRIVATE LIMITED·08904340408194·VELNEZ Nasal Pack 6 cm x 2 cm

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197056076·Stille Kidney Pedicle Clamp 230mm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197056069·Museux tonsil holding forceps, 200mm,...

NOVA STATSTRIP LACTATE HOSPITAL METER, NOVA STATSTRIP LACTATE TEST STRIPS

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SURELINE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS

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

LOGIC FEMORAL PS POR RIGHT SZ 2

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

BD LUER-LOK¿ TIP SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 15, 2023

BD LUER-LOK¿ TIP SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 15, 2023

LOGIC CR FEMORAL POR, LEFT, SZ 3.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 31, 2013

GEM PREMIER 4000

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code MZV·June 16, 2011

COAGUCHEK S SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·August 28, 2008

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023

ENDOSKELETON® TT CURVED, INSERTER

FDA Adverse Event
Malfunction ·TITAN SPINE, LLC·Product code LXH·July 14, 2016