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Sign in to claim this brandNeomend, Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 60 Technology Dr, Irvine, CA, 92618
- Website
- bd.com
- —
- —
- [email protected]
- Phone
- +1(888)776-4351
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3001237235
- DUNS Number
- 195251595
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Progel | PGEN005-11 | FDA UDI | Class III | Active |
| Progel | PGEN005-06 | FDA UDI | Class III | Active |
| Progel | PGST009 | FDA UDI | Class III | Active |
| Tridyne | TDET0006 | FDA UDI | Class III | Active |
| Tridyne | TDVS004 | FDA UDI | Class III | Active |
| Progel | PGPS002 | FDA UDI | Class III | Active |
| Tridyne | TDST0020 | FDA UDI | Class III | Active |
| Tridyne Vascular Sealant | P150016 | FDA PMA | Class III | Active |
| Neomend Progel Pleural Air Leak Sealant | P010047 | FDA PMA | Class III | Active |
Related Companies
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Authorities
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FDA Recalls (1)
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 |
|---|---|---|---|---|
| Aug 13, 2012 | Z-2454-2012 | — | terminated | Product was distributed with an incorrect expiration date. Product was labeled with an expiration date of 2013-04 and should have been labeled with 2012-09. |