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Depuy Spine, Inc.

US

Last updated September 17, 2026

Information

Country
US
Address
325 Paramount Drive, RAYNHAM, MA, 02767
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1526439
DUNS Number
—

Catalogue (4164)

Page 1 of 84
DeviceModel / ReferenceRegistriesClassStatus
Vsp 202544
FDA UDI
Class IUnknown
Expedium 186200001
FDA UDI
Class IIUnknown
Expedium 279752550
FDA UDI
Class IActive
Isola 205043
FDA UDI
Class IUnknown
Expedium 186202040
FDA UDI
Class IIUnknown
Vsp 30263250
FDA UDI
Class IIUnknown
Expedium 186254650L
FDA UDI
Class IIUnknown
Isola 500059000
FDA UDI
Class IIUnknown
Expedium 279792107
FDA UDI
Class IActive
Expedium 286280160
FDA UDI
Class IActive
Expedium 188183735
FDA UDI
Class IIUnknown
Isola 50112450
FDA UDI
Class IIUnknown
Mountaineer 288390220
FDA UDI
Class IActive
Expedium 279783120
FDA UDI
Class IActive
Expedium 186142425
FDA UDI
Class IIActive
Vsp 22262835
FDA UDI
Class IIUnknown
Moss 279720750
FDA UDI
Class IUnknown
Isola 223008
FDA UDI
Class IIUnknown
Vsp 202596
FDA UDI
Class IUnknown
Expedium 186188020
FDA UDI
Class IIActive
Moss 274219000
FDA UDI
Class IUnknown
Bremer AC014
FDA UDI
Class IIUnknown
Monarch 177036255
FDA UDI
Class IIUnknown
Expedium 188112525
FDA UDI
Class IIUnknown
Kaneda Sr 52113250
FDA UDI
Class IIUnknown
Expedium 186200003
FDA UDI
Class IIUnknown
Expedium 188112445
FDA UDI
Class IIUnknown
Alif Vertigraft 273513216
FDA UDI
Class IActive
Summit 274690300
FDA UDI
Class IActive
X-Mesh 288900008
FDA UDI
Class IUnknown
Keystone 282112415
FDA UDI
Class IActive
Bengal 177300164
FDA UDI
Class IIActive
Isola 203039
FDA UDI
Class IIUnknown
Summit 274669100
FDA UDI
Class IUnknown
Plif 273140000
FDA UDI
Class IUnknown
Expedium Sfx 189402210
FDA UDI
Class IIUnknown
Isola 50112440
FDA UDI
Class IIUnknown
Expedium 186253240
FDA UDI
Class IIUnknown
Summit 274654200
FDA UDI
Class IUnknown
Monarch 177067660
FDA UDI
Class IIUnknown
Keystone 282180411
FDA UDI
Class IActive
Mountaineer 288305120
FDA UDI
Class IUnknown
Expedium 279782850
FDA UDI
Class IActive
Viper 286705220
FDA UDI
Class IActive
Keystone 282101406
FDA UDI
Class IActive
Plif 20281809
FDA UDI
Class IActive
Expedium 188102850
FDA UDI
Class IIUnknown
Saber Lumbar I/F Cage 287007007
FDA UDI
Class IUnknown
Saber Lumbar I/F Cage 287014008
FDA UDI
Class IUnknown
Expedium 188132435
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (57)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
May 20, 2022Z-1324-2022—open, classified

Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton

May 20, 2022Z-1323-2022—open, classified

Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton

Apr 8, 2019Z-1225-2019—terminated

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

Apr 8, 2019Z-1226-2019—terminated

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

Dec 15, 2017Z-1300-2018—terminated

Certain lots of the spinal cement may contain incorrect amounts of contrast medium so that the product is difficult or impossible to visualize on x-ray.

Oct 12, 2016Z-0627-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Oct 12, 2016Z-0628-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Oct 12, 2016Z-0629-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Oct 12, 2016Z-0624-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Oct 12, 2016Z-0626-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Oct 12, 2016Z-0625-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Oct 12, 2016Z-0630-2017—terminated

SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging.

Nov 20, 2015Z-0454-2016—terminated

Manufacturing error within the Torque Handle may prohibit some handles from being able to fully assemble with the tightener shaft. The design of the inspection gage does not account for the additional shift length

Apr 21, 2015Z-1674-2015—terminated

Device does not mate as intended.

Jul 31, 2013Z-0096-2014—terminated

Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

Jul 31, 2013Z-0095-2014—terminated

Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

Jul 31, 2013Z-0093-2014—terminated

Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

Jul 31, 2013Z-0097-2014—terminated

Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

Jul 31, 2013Z-0094-2014—terminated

Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

Apr 17, 2013Z-2132-2013—terminated

During injection of cement, the water in the hydraulic pump leaks past the piston within the pump body resulting in the loss of pressure and inability to continue to inject cement.

Apr 17, 2013Z-2134-2013—terminated

During injection of cement, the water in the hydraulic pump leaks past the piston within the pump body resulting in the loss of pressure and inability to continue to inject cement.

Apr 17, 2013Z-2133-2013—terminated

During injection of cement, the water in the hydraulic pump leaks past the piston within the pump body resulting in the loss of pressure and inability to continue to inject cement.

Jan 15, 2013Z-0963-2013—terminated

Cement mixer used to prepare cement for surgery may not turn properly and may jam or stuck

Jan 15, 2013Z-0961-2013—terminated

Cement mixer used to prepare cement for surgery may not turn properly and may jam or stuck

Jan 15, 2013Z-0960-2013—terminated

Cement mixer used to prepare cement for surgery may not turn properly and may jam or stuck

Jan 15, 2013Z-0962-2013—terminated

Cement mixer used to prepare cement for surgery may not turn properly and may jam or stuck

Nov 7, 2012Z-0708-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0707-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0706-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0705-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0710-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0713-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the ilium. VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head.

Nov 7, 2012Z-0709-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0711-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Nov 7, 2012Z-0712-2013—terminated

Polyaxial screws 8x 80 and larger may disassociate when inserting in the Ilium., VIPER large diameter long screws in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head

Jul 24, 2012Z-0685-2013—terminated

A component within the handle of the Expedium Offset Torque Wrench is prematurely wearing, potentially resulting in the instrument recording torque values outside of the specification.

Mar 22, 2011Z-2102-2011—terminated

Mislabeled: Package labeled (11g x 6 inch) contains a 13g x 4-inch side hole needle

Mar 22, 2011Z-2103-2011—terminated

Mislabeled: Package labeled (11g x 6 inch) contains a 13g x 4-inch side hole needle

Oct 2, 2010Z-0818-2011—terminated

The scale which serves as a secondary means of identifying screw length is incorrectly etched on the screw caddy

Oct 2, 2010Z-0819-2011—terminated

The scale which serves as a secondary means of identifying screw length is incorrectly etched on the screw caddy

Oct 2, 2010Z-0817-2011—terminated

The scale which serves as a secondary means of identifying screw length is incorrectly etched on the screw caddy

Feb 11, 2009Z-1670-2009—terminated

Tip of Driver may break during use

Oct 10, 2006Z-0134-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0136-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0143-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0130-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0138-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0140-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0135-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0133-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0131-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0132-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0141-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0142-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0144-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0139-2007—terminated

Sterility of device is compromised due to loss of package integrity

Oct 10, 2006Z-0137-2007—terminated

Sterility of device is compromised due to loss of package integrity