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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

KIVA VCF TREATMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Batrik Pin Guard\.141"\Brown

FDA UDI
Batrik Medical Manufacturing Inc·00690521011205·Pin Guard, .141" (3.58 mm), Brown, Non-sterile

Batrik Pin-Kaps

FDA UDI
Batrik Medical Manufacturing Inc·00690521014206·Pin-Kaps, Sterile, Brown, 0.141" / 3.58 mm

Batrik Pin Guard\.141"\Brown w/sleeve

FDA UDI
Batrik Medical Manufacturing Inc·00690521014596·Pin Guard, .141" (3.58 mm), Brown, Non-sterile,...

DENTSPLY CAVITRON JET WAVE AIR POLISHING PROPHYLAXIS SYSTEM, MODEL G125

FDA 510(k)
FDA Class 1 ·Dental

SEILER COLPOSCOPE, MODELS 935, 955 AND 985

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ARCHITECT C4000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·September 16, 2020

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Death ·COOK VANDERGRIFT INC·Product code DRE·June 30, 2021

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Death ·COOK VANDERGRIFT INC·Product code DRE·June 30, 2021

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VASCULAR INC.·Product code DRE·January 8, 2018

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code DRE·February 15, 2022

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code DRE·November 6, 2017

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code DRE·December 15, 2017

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code DRE·November 29, 2017

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code DRE·October 5, 2018

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Death ·COOK VANDERGRIFT INC·Product code DRE·May 18, 2023

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code DRE·October 25, 2022

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code DRE·March 3, 2022

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code DRE·June 29, 2022

LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code DRE·June 8, 2022