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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 5 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ventralight | 5991525 | FDA UDI | Class II | Active |
| Xenmatrix | 1150606 | FDA UDI | Class II | Active |
| Sepramesh | 5959124 | FDA UDI | Class II | Active |
| Visilex | 0112910 | FDA UDI | Class II | Unknown |
| 3dmax | 0116310 | FDA UDI | Class II | Active |
| Phasix | 1191025 | FDA UDI | Class II | Active |
| Suretrans | 8594000 | FDA UDI | Class II | Active |
| Phasix | 1194040 | FDA UDI | Class II | Active |
| Sepramesh | 5959360 | FDA UDI | Class II | Active |
| Phasix | 1223035 | FDA UDI | Class II | Active |
| Phasix | 1201010 | FDA UDI | Class II | Active |
| Reconix | 0114115 | FDA UDI | Class II | Unknown |
| Arista | SM0005-USA | FDA UDI | Class III | Active |
| Hydro-Surg | 0026880 | FDA UDI | Class II | Active |
| Collamend | 1175113 | FDA UDI | Class II | Unknown |
| Endo-Flo | 0043950 | FDA UDI | Class II | Active |
| Bard | 0117841 | FDA UDI | Class II | Unknown |
| Dulex | 0126342 | FDA UDI | Class II | Unknown |
| Xenmatrix | 1162040 | FDA UDI | Class II | Active |
| Phasix | 1222025 | FDA UDI | Class II | Active |
| Simpulse | 0067570 | FDA UDI | Class II | Active |
| Simpulse | 0067320 | FDA UDI | Class II | Active |
| Avitene | 1050040 | FDA UDI | Class III | Active |
| Dulex | 0126341 | FDA UDI | Class II | Unknown |
| Onflex | 0115411 | FDA UDI | Class II | Active |
| 3dmax | 0115312 | FDA UDI | Class II | Active |
| Arista | AM0010 | FDA UDI | Class III | Active |
| Phasix | 1210020 | FDA UDI | Class II | Active |
| Hydro-Surg | 5536900 | FDA UDI | Class II | Unknown |
| Phasix | 1220812 | FDA UDI | Class II | Active |
| Phasix | 1194545 | FDA UDI | Class II | Active |
| Ventralight | 5954610 | FDA UDI | Class II | Active |
| Dulex | 0120301 | FDA UDI | Class II | Unknown |
| Dulex | 0110152 | FDA UDI | Class II | Unknown |
| Xenmatrix | 1151020 | FDA UDI | Class II | Active |
| Phasix | 1191530 | FDA UDI | Class II | Active |
| Simpulse | 0067590 | FDA UDI | Class II | Active |
| Composix | 0134810 | FDA UDI | Class II | Active |
| Endo-Flo | 0037970 | FDA UDI | Class II | Active |
| Bard | 0112740 | FDA UDI | Class II | Active |
| Simpulse | 0057570 | FDA UDI | Class II | Active |
| Xenmatrix | 1150816 | FDA UDI | Class II | Active |
| PerFix | 0117150 | FDA UDI | Class II | Active |
| Xenmatrix | 1152020 | FDA UDI | Class II | Active |
| Ventralex | 5950008 | FDA UDI | Class II | Active |
| PerFix | 0117070 | FDA UDI | Class II | Active |
| Xenmatrix | 1163030 | FDA UDI | Class II | Active |
| Ventralight | 5954450 | FDA UDI | Class II | Active |
| Simpulse | 0067740 | FDA UDI | Class II | Active |
| Ventralight | 5954680 | 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. |