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Sign in to claim this brandDavol Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 160 New Boston St, WOBURN, MA, 01801
- Website
- bd.com
- —
- —
- [email protected]
- Phone
- +1(800)562-0027
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000120505
- DUNS Number
- 001191048
Catalogue (449)
Page 3 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ventralight | 5954800 | FDA UDI | Class II | Active |
| Hydro-Surg | 5106020 | FDA UDI | Class II | Active |
| Composix | 0144113 | FDA UDI | Class II | Unknown |
| PerFix | 0117180 | FDA UDI | Class II | Active |
| Simpulse | 0067860 | FDA UDI | Class II | Unknown |
| Dulex | 0118242 | FDA UDI | Class II | Unknown |
| 3dmax | 0115310 | FDA UDI | Class II | Active |
| PerFix | 0112980 | FDA UDI | Class II | Active |
| Ventralight | 5955600 | FDA UDI | Class II | Active |
| Simpulse | 0067030 | FDA UDI | Class II | Active |
| Hydro-Surg | 5542900 | FDA UDI | Class II | Unknown |
| PerFix | 0112780 | FDA UDI | Class II | Active |
| 3dmax | 0115322 | FDA UDI | Class II | Active |
| Bard | 0112660 | FDA UDI | Class II | Active |
| Ventrio | 5950030 | FDA UDI | Class II | Active |
| Hydro-Surg | 5600240 | FDA UDI | Class II | Active |
| Phasix | 1230008 | FDA UDI | Class II | Active |
| Arista | AM0005 | FDA UDI | Class III | Active |
| Ventralex | 5950009 | FDA UDI | Class II | Active |
| 3dmax | 0115321 | FDA UDI | Class II | Active |
| Ventralight | 5954600 | FDA UDI | Class II | Active |
| Avitene | 1010110 | FDA UDI | Class III | Active |
| Composix | 0144114 | FDA UDI | Class II | Unknown |
| Kugel | 0010103 | FDA UDI | Class II | Active |
| Avitene | 1050030 | FDA UDI | Class III | Active |
| Phasix | 1190400 | FDA UDI | Class II | Active |
| Hemaderm | ENT0001-2 | FDA UDI | Class II | Active |
| Capsure | 0113215 | FDA UDI | Class II | Active |
| Ventralight | 5954790 | FDA UDI | Class II | Active |
| Ventralight | 5955680 | FDA UDI | Class II | Active |
| Phasix | 1202025 | FDA UDI | Class II | Active |
| Optifix | 0113320 | FDA UDI | Class II | Active |
| Phasix | 1211015 | FDA UDI | Class II | Active |
| Hydro-Surg | 0038140 | FDA UDI | Class II | Active |
| Ventralight | 5954810 | FDA UDI | Class II | Active |
| Bard | 0117010 | FDA UDI | Class II | Active |
| PerFix | 0112770 | FDA UDI | Class II | Active |
| Hydro-Surg | 5540220 | FDA UDI | Class II | Active |
| Arista | AM0004 | FDA UDI | Class III | Active |
| Bard | 0117013 | FDA UDI | Class II | Active |
| Avitene | 1010090 | FDA UDI | Class III | Active |
| Kugel | 0115814 | FDA UDI | Class II | Active |
| Simpulse | 0067910 | FDA UDI | Class II | Active |
| Xenmatrix | 1162025 | FDA UDI | Class II | Active |
| Avitene | 1020010 | FDA UDI | Class III | Active |
| Ventralight | 5955113 | FDA UDI | Class II | Active |
| Kugel | 0010104 | FDA UDI | Class II | Active |
| Composix | 0134680 | FDA UDI | Class II | Active |
| Phasix | 1210011 | FDA UDI | Class II | Active |
| Ventralight | 5992533 | FDA UDI | Class II | Active |
Related Companies
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 25, 2026 | Z-1896-2026 | — | open, classified | Potential for product to contain foreign matter, confirmed to be inspect fragments. |
| Apr 25, 2023 | Z-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, 2023 | Z-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, 2023 | Z-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, 2023 | Z-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, 2022 | Z-1457-2022 | — | open, classified | The device may potentially cause a fire, leading to a safety risk. |
| Jun 7, 2022 | Z-1305-2022 | — | open, classified | The product is not able to provide irrigation. |
| Jun 7, 2022 | Z-1304-2022 | — | open, classified | The product is not able to provide irrigation. |