21 results · 20ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Clinical Chemistry Prealbumin, List Number 1E02-20

FDA Recall
Terminated ·Abbott Laboratories Diagnostic Div·Product code JZJ·November 10, 2005

Thermoplastic templates, single tooth Catalog Number: 040.526

FDA Recall
Terminated ·Straumann Manufacturing Inc.·Product code DZJ·January 30, 2006

Stryker brand Consolidated Operating Room Equipment (CORE) System Powered Instrument Driver, REF 5400-50; Model 5400-050-000.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·August 5, 2005

Stryker brand Consolidated Operating Room Equipment (CORE) SystemPowered Instrument Driver, REF 5400-50; Model 5400-050-000A.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·August 5, 2005

Right/Left IBO Blade Set, for use with Stryker TPS Reciprocating Saw, REF 5100-37-903, Stryker Instruments, Kalamazoo, MI. Product Usage: The intended use of these devices is to cut bone and hard tissue in maxillofacial procedures and have been specifically designed for osteotomies of the mandibular ramus.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·October 18, 2011

Thermoplastic templates, free-end situation Catalog Number: 040.527

FDA Recall
Terminated ·Straumann Manufacturing Inc.·Product code DZJ·January 30, 2006

Left IBO Blade , for use with Stryker TPS or Core Reciprocating Saw, REF 5100-37-902S2, Stryker Instruments, Kalamazoo, MI. Product Usage: The intended use of these devices is to cut bone and hard tissue in maxillofacial procedures and have been specifically designed for osteotomies of the mandibular ramus.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·October 18, 2011

Avazzia Med-Best Therapeutic Massager; Model: BEST AV-1; P/N #MB04182-103; manufactured by Avazzia, Inc., Dallas, TX 75240.

FDA Recall
Terminated ·Avazzia, Inc·Product code GZJ·June 29, 2007

IBO Blade, Right, for use with Stryker TPS Reciprocating Saw, REF 5100-37-901, Stryker Instruments, Kalamazoo, MI. Product Usage: The intended use of these devices is to cut bone and hard tissue in maxillofacial procedures and have been specifically designed for osteotomies of the mandibular ramus.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·October 18, 2011

REF 5100-088, TPS Micro Driver, For Use with Stryker Total Performance System Caution Federal Law (USA) restricts the device to use by or on the order of a physician Driver, Wire and Bone Drill; The Stryker Total Performance System (TPS) is intended for use in the cutting, drilling, reaming, decorticating and smoothing of bone and other bone related tissues for a variety of applications such as ENT, dental, orthopedic, maxillofacial, spinal, and plastic surgery. The instruments are also used in the placement of screws, wires, pins, and other fixation devices.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·October 2, 2013

Avazzia BEST-RSI; Model: BEST AV-1; P/N #RS04303-103; manufactured by Avazzia, Inc., Dallas, TX 75240.

FDA Recall
Terminated ·Avazzia, Inc·Product code GZJ·June 29, 2007

IBO Blade, Left, for use with Stryker TPS Reciprocating Saw, REF 5100-37-902, Stryker Instruments, Kalamazoo, MI. Product Usage: The intended use of these devices is to cut bone and hard tissue in maxillofacial procedures and have been specifically designed for osteotomies of the mandibular ramus.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·October 18, 2011

Right IBO Blade , for use with Stryker TPS Reciprocating Saw, REF 5100-37-901S2, Stryker Instruments, Kalamazoo, MI. Product Usage: The intended use of these devices is to cut bone and hard tissue in maxillofacial procedures and have been specifically designed for osteotomies of the mandibular ramus.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code DZJ·October 18, 2011

Inter x 5002 Device, Inter x Professional Sport Device, Inter x 1000 Personal Device, and Inter x Personal Sport packaged with Triad alcohol wipes. The alcohol wipes manufactured by the Triad Group were labeled under brand names Triad, Select, Select Medical Products, PSS Select or PSS World Medical Inc. Alcohol wipe is provided as a cleaning convenience for device electrodes.

FDA Recall
Terminated ·Neuro Resource Group Inc·Product code GZJ·February 7, 2011

Synaptic 3600 and 3800 with Cranial Electrical Stimulation manufactured by Synaptic USA, Aurora, CO. Transcutaneous nerve stimulation for pain relief and other medical treatment uses.

FDA Recall
Terminated ·Synaptic Corp·Product code GZJ·July 18, 2008

Avazzia Tennant Biomodulator; Model: BEST AV-1; P/N #TB04303-103; manufactured by Avazzia, Inc., Dallas, TX 75240.

FDA Recall
Terminated ·Avazzia, Inc·Product code GZJ·June 29, 2007

Avazzia Med-Sport Massager; Model: BEST AV-1; P/N #MS04182-103; manufactured by Avazzia, Inc., Dallas, TX 75240.

FDA Recall
Terminated ·Avazzia, Inc·Product code GZJ·June 29, 2007

Line Powered RePak, Model Number 1785S

FDA Recall
Terminated ·Product code GZJ·May 23, 2003

Optetrak Constrained Condylar Offset Screw, Size JJ, Ref 208-04-77, Sterile, RX.

FDA Recall
Terminated ·Exactech, Inc.·Product code JWH·September 19, 2017

Optetrak Constrained Condylar Offset Screw, Size JJ, Ref 208-04-77, Sterile, RX.

FDA Enforcement
Class II ·Terminated·Exactech, Inc.·November 29, 2017