723 results
·
90ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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