37 results · 26ms · Sources: EU EUDAMED, US FDA

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Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Poly Stim II

FDA UDI
COMPASS HEALTH BRANDS CORP.·00850958007411·2"x2" Foam

Poly Stim II

FDA UDI
COMPASS HEALTH BRANDS CORP.·10850958007418·2"x2" Foam, Case of 10

Medidcal Science Products Private Label

FDA UDI
COMPASS HEALTH BRANDS CORP.·00092237900451·2"x2" Foam

MUST LT 25MM LONG - PEDICLE SCREW Ø6X45 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·January 19, 2024

KALAZAR DETECT

FDA 510(k)
FDA Class 1 ·Microbiology

MODIFIED HYDROPHILIC COATED GUIDEWIRE (STAINLESS STEEL CORE)

FDA 510(k)
FDA Class 2 ·Cardiovascular

MUST LT 03.57.035 MUST LT 15MM SHORT - PEDICLE SCREW Ø7X45 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 18, 2022

M.U.S.T. PEDICLE SCREW SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·September 18, 2025

PEDICLE SCREW MUST LT 15MM SHORT - PEDICLE SCREW Ø4.5X30 CANN

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 8, 2023

M.U.S.T. PEDICLE SCREW SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·July 16, 2025

MUST LT 03.59.234 MUST LT 25MM LONG - PEDICLE SCREW Ø7X40 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·February 16, 2022

MUST LT 15MM SHORT - PEDICLE SCREW Ø8X40 CANN

FDA Adverse Event
Death ·MEDACTA INTERNATIONAL SA·Product code NKB·March 29, 2023

MODULAR ANALYTICS CORE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 17, 2008

CAPSURE SP NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

MUST LT MUST LT 25MM LONG - PEDICLE SCREW 6X45 CANN

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·July 7, 2021

MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

FDA Recall
Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

SNAPLOC WIRE GUIDE LOCKING DEVICE

FDA Adverse Event
Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·December 18, 2024

SNAPLOC WIRE GUIDE LOCKING DEVICE

FDA Adverse Event
Malfunction ·WILSON-COOK MEDICAL INC·Product code ODC·December 16, 2024