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MICRO MEDICAL DEVICES, INC.

FDA registration
MICRO MEDICAL DEVICES, INC.·11 products·🇺🇸 United States

PalmScan PM2000

FDA UDI
Micro Medical Devices, Inc.·00853569007115·Advanced VR Pupilometer PUPILLOGRAPH

PalmScan K2000

FDA UDI
Micro Medical Devices, Inc.·00853569007047·Portable Keratometer TOPOGRAPHER, CORNEAL, BATT...

PalmScan AP2000

FDA UDI
Micro Medical Devices, Inc.·00853569007030·A 2000 portable A-scan biometer; AP 2000 Portab...

PalmScan P2000

FDA UDI
Micro Medical Devices, Inc.·00853569007016·P 2000 Portable Pachymeter Classification Name:...

PalmScan A2000 Pro with IOL Calculator

FDA UDI
Micro Medical Devices, Inc.·00853569007009·A2000 Portable A-Scan Ultrasonic or Ophthalmic ...

PalmScan DA2000

FDA UDI
Micro Medical Devices, Inc.·00853569007122·Dark Adaptometer

PalmScan VS2000

FDA UDI
Micro Medical Devices, Inc.·00853569007146·Visual Screening, DIGITAL VISUAL ACUITY TEST

PalmScan P2000FP

FDA UDI
Micro Medical Devices, Inc.·00853569007023·P2000 FP is a Portable Pachymeter SYSTEM, IMA...

PalmScan VF2000

FDA UDI
Micro Medical Devices, Inc.·00853569007108·Virtual reality based battery powered automatic...

PALMSCAN AP2000

FDA Adverse Event
Other ·MICRO MEDICAL DEVICES INC.·Product code IYO·April 22, 2009

PALM SCAN VF2000 G2

FDA Adverse Event
Injury ·MICRO MEDICAL DEVICES, INC.·Product code HPT·February 22, 2022

APEX¿

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL INC·Product code NEP·February 2, 2018

Microseal Augmented (20 degrees) Liner, acetabular liner component made from UHMW polyethylene (ASTM F648). Sizes 36x52x20; and 36x50x20. Device is intended for use with Whiteside Biomechanics, Inc./Signal Medical Corporation Micro-Seal Shell in an uncemented Total Hip Replacement.

FDA Enforcement
Class II ·Terminated·Signal Medical Corporation·October 29, 2014

AVANOS MEDICAL, INC

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code BTR·October 8, 2024

QDOT MICRO¿ CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·November 22, 2024

QDOT MICRO¿ CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code OAE·May 5, 2025

QDOT MICRO

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code OAE·February 24, 2025

CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·June 29, 2022

QDOT MICRO¿ CATHETER

FDA Adverse Event
Death ·BIOSENSE WEBSTER INC·Product code OAE·April 8, 2024