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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 2 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Arista | SM0007-USA | FDA UDI | Class III | Active |
| Ventralight | 5954124 | FDA UDI | Class II | Active |
| Phasix | 1200011 | FDA UDI | Class II | Active |
| Xenmatrix | 1152530 | FDA UDI | Class II | Active |
| Composix | 0144680 | FDA UDI | Class II | Unknown |
| Phasix | 1192030 | FDA UDI | Class II | Active |
| Sepramesh | 5959680 | FDA UDI | Class II | Active |
| Phasix | 1190500 | FDA UDI | Class II | Active |
| Phasix | 1211520 | FDA UDI | Class II | Active |
| PerFix | 0112970 | FDA UDI | Class II | Active |
| Phasix | 1211823 | FDA UDI | Class II | Active |
| Phasix | 1193045 | FDA UDI | Class II | Active |
| Simpulse | 0067020 | FDA UDI | Class II | Active |
| X-Stream | 5552000 | FDA UDI | Class II | Unknown |
| Hydro-Surg | 5600280 | FDA UDI | Class II | Active |
| Avitene | 1010010 | FDA UDI | Class III | Active |
| Composix | 0123460 | FDA UDI | Class II | Active |
| Ventralight | 5955450 | FDA UDI | Class II | Active |
| Avitene | 1010260 | FDA UDI | Class III | Unknown |
| Sepramesh | 5959480 | FDA UDI | Class II | Active |
| 3dmax | 0116322 | FDA UDI | Class II | Active |
| Kugel | 0010105 | FDA UDI | Class II | Active |
| Xenmatrix | 1151530 | FDA UDI | Class II | Active |
| Xenmatrix | 1151935 | FDA UDI | Class II | Active |
| Dulex | 0115192 | FDA UDI | Class II | Unknown |
| Bard | 0117009 | FDA UDI | Class II | Active |
| 3dmax | 0117321 | FDA UDI | Class II | Active |
| Phasix | 1191010 | FDA UDI | Class II | Active |
| 3dmax | 0115320 | FDA UDI | Class II | Active |
| Simpulse | 0057700 | FDA UDI | Class II | Unknown |
| Dulex | 0108121 | FDA UDI | Class II | Unknown |
| Phasix | 1190808 | FDA UDI | Class II | Active |
| Ventrio | 5950080 | FDA UDI | Class II | Active |
| X-Stream | 5552002 | FDA UDI | Class II | Unknown |
| Avitene | 1050020 | FDA UDI | Class III | Active |
| PerFix | 0117160 | FDA UDI | Class II | Active |
| PerFix | 0117060 | FDA UDI | Class II | Active |
| Phasix | 1191525 | FDA UDI | Class II | Active |
| Endo-Flo | 0025521 | FDA UDI | Class II | Active |
| Ventralex | 0010302 | FDA UDI | Class II | Active |
| Hydro-Surg | 0026870 | FDA UDI | Class II | Active |
| Phasix | 1220011 | FDA UDI | Class II | Active |
| Bard | 0117008 | FDA UDI | Class II | Active |
| Xenmatrix | 1152040 | FDA UDI | Class II | Active |
| Reconix | 0114510 | FDA UDI | Class II | Unknown |
| 3dmax | 0117312 | FDA UDI | Class II | Active |
| Phasix | 1190100 | FDA UDI | Class II | Active |
| Ventralex | 5950007 | FDA UDI | Class II | Active |
| Collamend | 1175114 | FDA UDI | Class II | Unknown |
| Ventrio | 0010214 | FDA UDI | Class II | Active |
Related Companies
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Importers
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Authorities
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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. |