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

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VERSACLOSE, MODEL VC-200-01

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

DEBAKEY VASCULAR CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921005720·DEBAKEY PEDIATRIC VASCULAR CLAMP SPOON JAW

HS Stand. Burr, Ø7.0x70, 80k

FDA UDI
Bien-Air Surgery SA·17630055507133·

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100552821·IN-OVATION® C EURO 022 U 5-5/L 3-3 CS-BC HK

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100552811·IN-OVATION® C EURO 022 U5-5/L3-3 CS HK

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532601·IN-OVATION® C Roncone 022/U5-5 L3-3 CS HK

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532001·IN-OVATION® C Base Rx 022 U5-5/L3-3

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532611·IN-OVATION® C Roncone 022/U5-5 L3-3 CS-BC HK

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532111·IN-OVATION® C Base Rx 022 U5-5/L3-3 CS-BC HK

IN-OVATION® C

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100532101·IN-OVATION® C Base Rx 022 U5-5/L3-3 CS HK

BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE

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

E.N.S.I. SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

Widex

FDA UDI
Widex A/S·05706069437164·Widex SUPER440 S4-VS BTE (Winter silver/Black )...

Widex

FDA UDI
Widex A/S·05706069409857·Widex SUPER220 S2-VS BTE (Winter silver/Black )...

STEM: SMS SOLID SMS SOLID STEM STD SIZE 5

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 22, 2022

BD Q-SYTE CLOSED LUER ACCESS DEVICE

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·April 29, 2025

BD Q-SYTE CLOSED LUER ACCESS DEVICE

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·April 29, 2025

QUANTUM Q6 EDGE WITH TB3 POWER SEATING SYSTEM

FDA Adverse Event
Malfunction ·PRIDE MOBILITY PRODUCTS CORP·Product code IOR·September 24, 2015

ENDEAVOR RESOLUTE RX

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code NIQ·September 19, 2014

FEMORAL AND PROVISIONAL IMPACTOR/EXTRACTOR

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code MBH·May 17, 2011