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Sign in to claim this brandDSM BIOMEDICAL, INC.
United States·US-MF-000021393
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 735, Pennsylvania Drive, Exton , United States
- —
- —
- [email protected]
- Phone
- +1 484 713 2100
- PRRC Contact
- Susan Pileggi
- EUDAMED SRN
- US-MF-000021393
- FDA FEI Number
- 1000307073
- DUNS Number
- 131107757
Catalogue (181)
Page 2 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Meso Dental Membrane | 30053-07 | FDA UDI | Class II | Active |
| CopiOs® Bone Void Filler Paste | 20102-01 | FDA UDI | Class II | Active |
| Resolve Matrix™ Biologic Membrane | 30052-22 | FDA UDI | U | Active |
| TrelliForm | 30017-03 | FDA UDI | Class II | Unknown |
| CopiOs® Bone Void Filler Paste | 20102-03 | FDA UDI | Class II | Active |
| DSM Biomedical Dental Bone Graft | 30070-09 | FDA UDI | Class II | Active |
| Renovix-Plus | 30072-04 | FDA UDI | Class II | Active |
| WizardBio Resorbable Calcium Phosphate Cement | 21004-10 | FDA UDI | Class II | Unknown |
| DSM Biomedical Dental Bone Graft | 30070-07 | FDA UDI | Class II | Active |
| Meso BIlayer Surgical Mesh | 30060-06 | FDA UDI | Class II | Unknown |
| Meso Bilayer Surgical Mesh | 30060-01 | FDA UDI | Class II | Unknown |
| ProChondrix® Sizer Set | 58161-02 | FDA UDI | Class I | Unknown |
| Meso Wound Matrix | 30052-14 | FDA UDI | U | Active |
| TrelliForm | 30017-02 | FDA UDI | Class II | Unknown |
| EpiGuide® Bioresorbable Barrier Matrix | 50600-02 | FDA UDI | Class II | Unknown |
| TrelliForm | 30017-04 | FDA UDI | Class II | Unknown |
| XCM Biologic® Tissue Matrix | 30010-04 | FDA UDI | Class II | Active |
| Osseofit™ Porous Tissue Matrix | 50604-10 | FDA UDI | Class II | Unknown |
| PEAK® Platelet Rich Plasma System | 64000-01 | FDA UDI | Class II | Active |
| SalvinOSS Collagen Xenograft and Collagen Bone Graft Material | 30069-02 | FDA UDI | Class II | Active |
| Meso BioMatrix® Acellular Peritoneum Matrix | 30063-03 | FDA UDI | Class II | Active |
| Resolve Matrix™ Biologic Membrane | 30052-27 | FDA UDI | U | Active |
| Meso Dental Membrane | 30053-06 | FDA UDI | Class II | Active |
| XCM Biologic® Tissue Matrix | 30010-09 | FDA UDI | Class II | Active |
| CopiOs® Bone Void Filler Paste | 20102-02 | FDA UDI | Class II | Active |
| GENIUS Platelet Rich Plasma (PRP) System | 64000-05 | FDA UDI | Class II | Unknown |
| Arthrex DX Reinforcement Matrix | 30030-02 | FDA UDI | Class II | Active |
| Meso Dental Membrane | 30053-04 | FDA UDI | Class II | Active |
| Resolve Matrix™ Biologic Membrane | 30052-25 | FDA UDI | U | Active |
| Arthrex DX Reinforcement Matrix | 30030-01 | FDA UDI | Class II | Active |
| TrelliForm | 30017-06 | FDA UDI | Class II | Unknown |
| Meso BioMatrix® Acellular Peritoneum Matrix | 30063-01 | FDA UDI | Class II | Active |
| DSM Biomedical Centrifuge | 64002-08 | FDA UDI | Class II | Active |
| CopiOs® Bone Void Filler Sponge | 20100-03 | FDA UDI | Class II | Active |
| Resolve Matrix™ Biologic Membrane | 30052-30 | FDA UDI | U | Active |
| Arthrex DX Reinforcement Matrix | 30030-01 | FDA UDI | Class II | Active |
| Renovix-Plus | 30072-01 | FDA UDI | Class II | Active |
| BoneSync Fast-Setting Drillable Calcium Phosphate Cement | 21003-10 | FDA UDI | Class II | Active |
| Resolve Matrix™ Biologic Membrane | 30052-23 | FDA UDI | U | Active |
| CopiOs® Bone Void Filler Sponge | 20101-01 | FDA UDI | Class II | Active |
| Osseofit™ Porous Tissue Matrix | 50604-12 | FDA UDI | Class II | Unknown |
| CopiOs® Bone Void Filler Sponge | 20100-01 | FDA UDI | Class II | Active |
| GENIUS Blood and Marrow Concentration (BM/C) System | 64150-04 | FDA UDI | Class II | Active |
| CopiOs® Bone Void Filler Paste | 20102-01 | FDA UDI | Class II | Active |
| OptiMatrix™ Extracellular Matrix | 30053-01 | FDA UDI | Class II | Unknown |
| Renovix-Plus | 30072-02 | FDA UDI | Class II | Active |
| CopiOs® Bone Void Filler Paste | 20102-03 | FDA UDI | Class II | Active |
| Meso BioMatrix® Acellular Peritoneum Matrix | 30063-02 | FDA UDI | Class II | Active |
| CopiOs® Bone Void Filler Sponge | 20100-02 | FDA UDI | Class II | Active |
| Resolve Matrix™ Biologic Membrane | 30052-21 | FDA UDI | U | Active |
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