62 results · 12ms · Sources: EU EUDAMED, US FDA

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Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML, Part ID 16815

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035

FDA Enforcement
Class II ·Terminated·BioPro, Inc.·March 9, 2022

MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

FDA Recall
Terminated ·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code LQC·January 4, 2021

MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-244 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

FDA Recall
Terminated ·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code LQC·January 4, 2021

MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

FDA Enforcement
Class II ·Terminated·Aomori Olympus Co., Ltd.·February 17, 2021

MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-244 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.

FDA Enforcement
Class II ·Terminated·Aomori Olympus Co., Ltd.·February 17, 2021

Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible endoscopes include Olympus bronchoscopes, cystoscopes, rhino-laryngoscopes and pleurascopes models.

FDA Enforcement
Class II ·Terminated·Olympus Corporation of the Americas·August 14, 2019

Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylinder of compatible endoscopes for aspirating fluid from the distal end of the endoscopes through the instrument channel. Compatible endoscopes include Olympus bronchoscopes, cystoscopes, rhino-laryngoscopes and pleurascopes models.

FDA Recall
Terminated ·Olympus Corporation of the Americas·Product code EOQ·April 1, 2019

Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664

FDA Recall
Terminated ·Olympus Corporation of the Americas·Product code FEM·June 10, 2019

Left Locking 2st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: Left Locking 2st MTP/MPJ Combo Fusion Plate... REF 70-0036-S... LOT W58123".

FDA Recall
Terminated ·Acumed LLC·Product code HWC·February 14, 2008

Right Locking 1st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: Right Locking 1st MTP/MPJ Combo Fusion Plate... REF 70-0037-S... LOT W58148".

FDA Recall
Terminated ·Acumed LLC·Product code HWC·February 14, 2008

Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source, documentation equipment, monitor, Endo Therapy accessories (such as biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.

FDA Recall
Terminated ·Olympus Corporation of the Americas·Product code FDT·January 28, 2021