28 results · 21ms · 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.

MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032

FDA Recall
Terminated ·Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany·Product code FTM·December 29, 2021

.045 X 6 ST Guide Wire, Part number 45-0029-S, Sterile 10 pack of WS-1106ST and has a 6 inch length and 0.045 inch diameter. .054 X 7 ST Guide Wire, Part number 45-0031-S, Sterile 10 Pack of WS-1407ST and has a 7 inch length and 0.054 inch diameter. These guide wires are an orthopedic manual surgical instrument.

FDA Recall
Terminated ·Acumed LLC·Product code LXH·February 17, 2017

Edwards Lifesciences Fogaty Occlusion Catheter Ref # 62080822F. The product is intended for use in Temporary Vessel Occlusion.

FDA Recall
Terminated ·Edwards Lifesciences, Llc·Product code MFC·June 22, 2009

Spirit MB Brackets, part #494-1211. The brand name of the device is Spirit MB Brackets, an orthodontic bracket. Spirit MB Brackets have been assigned the product code 76 DYW (Plastic Orthodontic Bracket) by the FDA and is classified as a Class II Medical Device. Spirit MB Brackets are to be fixed attachment on a tooth which holds an archwire during orthodontic treatment.

FDA Recall
Terminated ·Ormco Corporation·Product code DYW·May 18, 2011

Spirit MB Brackets, part #494-1210. The brand name of the device is Spirit MB Brackets, an orthodontic bracket. Spirit MB Brackets have been assigned the product code 76 DYW (Plastic Orthodontic Bracket) by the FDA and is classified as a Class II Medical Device. Spirit MB Brackets are to be fixed attachment on a tooth which holds an archwire during orthodontic treatment.

FDA Recall
Terminated ·Ormco Corporation·Product code DYW·May 18, 2011

MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB) Right Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR BARRIER Implants are intended for the augmentation or restoration of bony contour in the craniofacial skeleton.

FDA Recall
Terminated ·Stryker Craniomaxillofacial Division·Product code FTL·December 17, 2014

Centurion-Medicine Cup GMC205 GLASS MEDICINE CUP 2 OUNCE STERILE

FDA Recall
Terminated ·Centurion Medical Products Corporation·Product code KYW·December 11, 2019

Medicine Cup, 1 OZ. Liquid medication dispenser to issue a measured amount of liquid medication.

FDA Recall
Terminated ·Medline Industries Inc·Product code KYW·May 11, 2016

Damon 3 Bracket Upper Right lateral .022 slot Part Number 491-4210 Lot Number100512025 and 100512020

FDA Recall
Terminated ·Ormco Corporation·Product code DYW·November 3, 2005

Rusch (Latex Free) Neoprene Pecan Shaped Breathing Bag with 15 mm neck insert, size 1 liter; a rebreathing bag; Teleflex Medical, Bannockburn, IL 60015 USA, Made in UK

FDA Recall
Terminated ·Teleflex Medical·Product code BYW·October 31, 2006

Spirit MB Bracket, UR Central +14T +5A.018, Part Number 494-0110, Lot Number 081351013. Product Usage: An orthodontic bracket. Spirit MB Brackets are a fixed attachment on a tooth which holds an archwire during orthodontic treatment.

FDA Recall
Terminated ·Ormco/Sybronendo·Product code DYW·March 25, 2014

Damon 3 Bracket Upper Right lateral .022 slot Part Number 491-4211 Lot Number 100514071 and 100512012

FDA Recall
Terminated ·Ormco Corporation·Product code DYW·November 3, 2005

Centurion-Pitcher Kit GR100150ST GRADUATED PITCHER STERILE 1000 CC Y 2018121090 GR1200ST STERILE 1200CC PITCHER KIT Y 2019031990

FDA Recall
Terminated ·Centurion Medical Products Corporation·Product code KYW·December 11, 2019

VC150 Vital Signs Monitor (VC150 monitor equipped with Masimo SpO2 technique only); Innokas Medical CARESCAPE VC150 Rx Only Innokas Medical Oy. Catalog numbers 2067980-002, 2067980-006, 2067980-010, and 2067980-014.

FDA Recall
Terminated ·INNOKAS MEDICAL OY TARJUSOJANTIE 12 KEMPELE Finland·Product code MWI·December 3, 2014

KaVo Scan eXam SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)

FDA Recall
Terminated ·Palodex Group Oy Nahkelantie 160 Tuusula Finland·Product code MQB·January 7, 2020

Gendex GXPS-500 SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)

FDA Recall
Terminated ·Palodex Group Oy Nahkelantie 160 Tuusula Finland·Product code MQB·January 7, 2020

CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.

FDA Recall
Terminated ·INNOKAS MEDICAL OY TARJUSOJANTIE 12 KEMPELE Finland·Product code MWI·July 27, 2016

CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans

FDA Recall
Terminated ·Innokas Medical Oy Vihikari 10 Kempele Finland·Product code MWI·October 22, 2015

Instrumentarium Dental Express SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)

FDA Recall
Terminated ·Palodex Group Oy Nahkelantie 160 Tuusula Finland·Product code MQB·January 7, 2020

Soredex DIGORA Optime SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)

FDA Recall
Terminated ·Palodex Group Oy Nahkelantie 160 Tuusula Finland·Product code MQB·January 7, 2020