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Davol Inc.

US

Last updated September 17, 2026

Information

Country
US
Address
160 New Boston St, WOBURN, MA, 01801
Website
bd.com
LinkedIn
—
Facebook
—
Phone
+1(800)562-0027
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1000120505
DUNS Number
001191048

Catalogue (449)

Page 6 of 9
DeviceModel / ReferenceRegistriesClassStatus
Hydro-Surg 5103010
FDA UDI
Class IIUnknown
Bard 0118004
FDA UDI
Class IIUnknown
Avitene 1050050
FDA UDI
Class IIIActive
Hydro-Surg 5101210
FDA UDI
Class IIActive
PerFix 0112760
FDA UDI
Class IIActive
Simpulse 0067621
FDA UDI
Class IIActive
Bard 0118001
FDA UDI
Class IIUnknown
Hydro-Surg 5600200
FDA UDI
Class IIActive
Hydro-Surg 5106115
FDA UDI
Class IIActive
Dulex 0110151
FDA UDI
Class IIUnknown
Ventrio 0010218
FDA UDI
Class IIActive
Xenmatrix 1152540
FDA UDI
Class IIActive
Phasix 1193030
FDA UDI
Class IIActive
Ventralight 5955810
FDA UDI
Class IIActive
Hydro-Surg 5600160
FDA UDI
Class IIUnknown
Ventrio 5950050
FDA UDI
Class IIActive
Dulex 0118241
FDA UDI
Class IIUnknown
3dmax 0116312
FDA UDI
Class IIActive
Xenmatrix 1150616
FDA UDI
Class IIActive
3dmax 0116311
FDA UDI
Class IIActive
Phasix 1191020
FDA UDI
Class IIActive
Phasix 1230007
FDA UDI
Class IIActive
Suretrans 8592000
FDA UDI
Class IIActive
Endo-Flo 0043970
FDA UDI
Class IIUnknown
Ventralight 5990020
FDA UDI
Class IIActive
Suretrans 8590000
FDA UDI
Class IIActive
Phasix 1190601
FDA UDI
Class IIActive
Bard 0112700
FDA UDI
Class IIActive
Phasix 1200710
FDA UDI
Class IIActive
Phasix 1201520
FDA UDI
Class IIActive
Nezhat-Dorsey 5202770
FDA UDI
Class IIActive
Optifix 0113126
FDA UDI
Class IIActive
Ventralight 5954460
FDA UDI
Class IIActive
3dmax 0115311
FDA UDI
Class IIActive
Ventrio 0010213
FDA UDI
Class IIActive
Xenmatrix 1161015
FDA UDI
Class IIActive
Xenmatrix 1161928
FDA UDI
Class IIActive
Ventrio 0010212
FDA UDI
Class IIActive
Phasix 1221520
FDA UDI
Class IIActive
Xenmatrix 1160610
FDA UDI
Class IIActive
Composix 0134610
FDA UDI
Class IIActive
Composix 0123790
FDA UDI
Class IIActive
Hydro-Surg 5600360
FDA UDI
Class IIActive
Phasix 1201325
FDA UDI
Class IIActive
Simpulse 0067690
FDA UDI
Class IIActive
Permafix 0113119
FDA UDI
Class IIActive
Phasix 1190816
FDA UDI
Class IIActive
Simpulse 0037640
FDA UDI
Class IIActive
Avitene 1010590
FDA UDI
Class IIIActive
Phasix 1190602
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (8)

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
Mar 25, 2026Z-1896-2026—open, classified

Potential for product to contain foreign matter, confirmed to be inspect fragments.

Apr 25, 2023Z-2242-2023—open, classified

Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection

Apr 25, 2023Z-2241-2023—open, classified

Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection

Apr 25, 2023Z-2244-2023—open, classified

Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection

Apr 25, 2023Z-2243-2023—open, classified

Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection

Jun 27, 2022Z-1457-2022—open, classified

The device may potentially cause a fire, leading to a safety risk.

Jun 7, 2022Z-1305-2022—open, classified

The product is not able to provide irrigation.

Jun 7, 2022Z-1304-2022—open, classified

The product is not able to provide irrigation.