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Sign in to claim this brandBIOCOMPOSITES LTD
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- biocomposites.com
- —
- —
- [email protected]
- Phone
- +441782338580
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 424382307
Catalogue (205)
Page 4 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Allogran-R® | 800-005 | FDA UDI | Class II | Active |
| Bilok® Screw | 160-825T | FDA UDI | Class II | Unknown |
| NanoBone® QD | 200073 | FDA UDI | Class II | Active |
| Bilok® Screw | 160-925T | FDA UDI | Class II | Unknown |
| NanoBone® SBX Putty | 200045 | FDA UDI | Class II | Active |
| Bilok® Screw | 160-725T | FDA UDI | Class II | Active |
| NanoBone® QD | 200077 | FDA UDI | Class II | Active |
| Bilok® Screw | 160-935T | FDA UDI | Class II | Unknown |
| Biosteon® Screw | 234-010-166 | FDA UDI | Class II | Active |
| Biosteon® Screw | 234-010-161 | FDA UDI | Class II | Active |
| Stimulan Kit 10cc (CHINA ONLY) | 600-010 | FDA UDI | Class II | Active |
| Stimulan® Rapid Cure | 620-010 | FDA UDI | Class II | Unknown |
| geneX® putty | 920-010 | FDA UDI | Class II | Unknown |
| Bilok® ST Screw | 160-930ST | FDA UDI | Class II | Active |
| Synicem Hip Spacer 40CXL | 885433 | FDA UDI | Class I | Active |
| Synicem Hip Spacer Trial Tray Regular with Trials | 882022 | FDA UDI | N/A | Active |
| Biosteon® IntraLine® | 3910-200-085 | FDA UDI | Class II | Active |
| Stimulan® DS | 640-005 | FDA UDI | Class II | Active |
| Synicem Shoulder Spacer Trial Tray with Trials | 882052 | FDA UDI | N/A | Active |
| Synicem 72 Knee Trial FDA | 885420 | FDA UDI | Class I | Active |
| Stimulan® Dispenser | 600-30-s1 | FDA UDI | Class II | Active |
| Synicem 65 Knee Trial FDA | 885419 | FDA UDI | Class I | Active |
| Biosteon® IntraLine® | 3910-200-086 | FDA UDI | Class II | Active |
| Synicem Hip Spacer 56M | 885437 | FDA UDI | Class I | Active |
| Synicem Hip Spacer 48C | 885431 | FDA UDI | Class I | Active |
| Synicem 79 Knee Trial FDA | 885421 | FDA UDI | Class I | Active |
| Synicem Knee Spacer R58 | 885438 | FDA UDI | Class I | Active |
| Biosteon® IntraLine® | 3910-200-084 | FDA UDI | Class II | Active |
| Allogran-R | K061311 | FDA 510(k) | Class II | Active |
| Little Grafter Screw | K040265 | FDA 510(k) | Class II | Active |
| Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer | K242865 | FDA 510(k) | Class II | Active |
| Modification To Bilok Screw | K071091 | FDA 510(k) | Class II | Active |
| Fortoss Vital Bone Graft Substitute | K050170 | FDA 510(k) | Class II | Active |
| Biolok Screw, Biosteon Screw | K003641 | FDA 510(k) | Class II | Active |
| Stimulan -calcium Sulfate Bone Void Filter | K001724 | FDA 510(k) | Class II | Active |
| Biosteon® Screw | K251680 | FDA 510(k) | Class II | Active |
| Dominator | K072127 | FDA 510(k) | Class II | Active |
| Stimulan - Calcium Sulfate Bone Void Filler Kit | K021551 | FDA 510(k) | Class II | Active |
| Biolok Screw | K002070 | FDA 510(k) | Class II | Active |
| Biosteon Cross Pin | K021351 | FDA 510(k) | Class II | Active |
| Modification To Bilok St Screw | K071115 | FDA 510(k) | Class II | Active |
| Genex Bone Graft Substitute | K040600 | FDA 510(k) | Class II | Active |
| Fortoss-Cema | K993238 | FDA 510(k) | Class II | Active |
| Stimulan - Calcium Sulfate Bone Void Filler Kit | K003954 | FDA 510(k) | Class II | Active |
| Bilok St Screw | K033792 | FDA 510(k) | Class II | Active |
| Stimulan Kit, Stimulan Rapid Cure | K141830 | FDA 510(k) | Class II | Active |
| Fortoss Vital | K082383 | FDA 510(k) | Class II | Active |
| Modification To Doubleplay Suture Anchor | K081428 | FDA 510(k) | Class II | Active |
| Genex Putty | K073341 | FDA 510(k)FDA UDI | Class II | Active |
| Doubleplay Suture Anchor | K061949 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Biocomposites Ltd. Keele Staffordshire · GB FEI 3002806534