54 results · 32ms · Sources: EU EUDAMED, US FDA

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36M - MSHA Miners

FDA UDI
Certified Safety Manufacturing, Inc.·00766588026206·36M - MSHA Miners

FlexCath Advance Steerable Sheath and Dilator

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
Synthes GmbH·10886982144317·3.0MM CANNULATED SCREW SHORT THREAD/20MM

Marking Pen

FDA UDI
KATENA PRODUCTS, INC.·00841668113219·MARKING PEN FOR TREPHINE & PUNCH

Medical Facets NC

FDA UDI
MEDICAL FACETS NC LLC·M933MDF2026200·3.0mm Cannulated Screw, Short Thread, 20mm

Diamond Orthopedic, LLC

FDA UDI
DIAMOND ORTHOPEDIC, LLC·B551DMD2026200·3.0mm, Cannulated Screw, Short Thd., 20mm

SHEATHLESS ACCESSORY KIT, MODELS XRIK24, XRIK28, XRIK32, XRIK36, XRIK40 AND XRIKRT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SURESMILE SYSTEM

FDA 510(k)
FDA Class 1 ·Dental

HEPARIN GRAFTED (EVODIAL)

FDA Adverse Event
Malfunction ·VANTIVE US HEALTHCARE LLC·Product code KDI·April 16, 2026

I-STAT CHEM8+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JPI·February 10, 2026

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 18, 2026

PUMP 1886 780G OUS BLE PUMP MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 25, 2026

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 4, 2026

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 3, 2026

POWERGLIDE PRO

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code FOZ·May 5, 2026

MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 6, 2026

STOCKERT CENTRIFUGAL PUMP CONSOLE

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code KFM·October 15, 2014

OMNISPAN MENISCAL FASTENER, 12 DEGREE

FDA Adverse Event
Malfunction ·DEPUY MITEK·Product code MBI·August 11, 2011

PINN 100 W/GRIPTION 52MM

FDA Adverse Event
Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·July 2, 2013

MMT-712 PARADIGM INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·January 22, 2026