16 results · 25ms · Sources: EU EUDAMED, US FDA

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Ion Endoluminal System

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112564·BARRON CORNEAL PUNCH 6.0MM

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113271·STAB KNIFE 15 DEGREE (BX/5)

Accufit

FDA UDI
Ortho Organizers, Inc.·00190707184148·Accufit Molar Bands Lower Left Second Molar 37

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113387·ALIO MICS TRAP KNIFE (BX/5)

FRAMELOCK; FRAMELOCK ACCESSORIES

FDA 510(k)
FDA Class 2 ·Neurology

R3 XLPE ANTEVERTED LINERS

FDA 510(k)
FDA Class 2 ·Orthopedic

BD SAFE-CLIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·May 5, 2021

NC EMERGE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 18, 2023

STAAR SURGICAL

FDA Adverse Event
Injury ·STAAR SURGICAL·Product code LZS·October 23, 2014

TRUFILL DCS ORBIT MINI COMPLEX FILL

FDA Adverse Event
Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·August 11, 2011

SYNCHROMED II

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

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 22, 2024

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 9, 2022

UNKNOWN EXTERNAL DRAINAGE AND MONITORING SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC MEXICO·Product code GWM·April 30, 2024

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012