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Sign in to claim this brandALTATEC GmbH
Germany·DE-MF-000006230
Last updated September 17, 2026
Information
- Country
- Germany
- Address
- 5, Maybachstr., Wimsheim, Germany
- Website
- www.altatec.de
- —
- —
- [email protected]
- Phone
- +49-70449445-311
- PRRC Contact
- Raphael Brausch
- EUDAMED SRN
- DE-MF-000006230
- FDA FEI Number
- 3002806355
- DUNS Number
- 322018193
Catalogue (2143)
Page 4 of 43| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CAMLOG® SCREW-LINE Implant, Promote® | K1044.3311 | FDA UDI | Class II | Unknown |
| CAMLOG® Impression post | K2121.3800 | FDA UDI | Class I | Active |
| CAMLOG® SCREW-LINE Implant, Promote® | K1042.4313 | FDA UDI | Class II | Unknown |
| Bar implant analog | J3025.4300 | FDA UDI | Class I | Active |
| Guide CONELOG® Insertion post | C2026.4300 | FDA UDI | Class I | Unknown |
| CONELOG® Bar abutment | C2255.4340 | FDA UDI | Class II | Unknown |
| Matrix CM Dalbo®-Plus | J2250.0005 | FDA UDI | Class II | Unknown |
| Guide Guiding sleeve, | J3734.6003 | FDA UDI | Class I | Unknown |
| CAMLOG® Healing Cap PS | K2001.6040 | FDA UDI | Class II | Unknown |
| Guide CAMLOG® Insertion post | K2026.5003 | FDA UDI | Class I | Active |
| CAMLOG® Titanium base, for CAMLOG® ceramic abutment | K2242.4342 | FDA UDI | Class II | Unknown |
| CAMLOG® SCREW-LINE Implant, Promote® | K1042.4311 | FDA UDI | Class II | Unknown |
| Guide Guiding sleeve, | J3734.5003 | FDA UDI | Class I | Unknown |
| CONELOG® Ball abutment set | C2250.5045 | FDA UDI | Class II | Unknown |
| Collet | J3712.4300 | FDA UDI | Class I | Active |
| CAMLOG® Impression post | K2119.3800 | FDA UDI | Class I | Active |
| Guide Template drill | J3753.5000 | FDA UDI | Class I | Active |
| Plaster cutter | J3706.6000 | FDA UDI | Class I | Active |
| Guide Template drill | J3733.3300 | FDA UDI | Class I | Active |
| Removal adapter, CONELOG® | C5302.5001 | FDA UDI | Class I | Unknown |
| CONELOG® SCREW-LINE Implant, Promote® plus | C1062.3311 | FDA UDI | Class II | Unknown |
| Guide CONELOG® SL Implant, Promote® plus | C1063.3313 | FDA UDI | Class II | Unknown |
| CAMLOG® Ceramic abutment | K2242.3340 | FDA UDI | Class II | Unknown |
| CAMLOG® Vario SR abutment | K2562.3800 | FDA UDI | Class II | Unknown |
| Vario SR protection cap | J2568.6000 | FDA UDI | Class II | Active |
| Guide CAMLOG® SL Implant, Promote® plus | K1053.3813 | FDA UDI | Class II | Unknown |
| Bite registration cap | J2112.6000 | FDA UDI | Class I | Active |
| CAMLOG® Bar abutment | J2255.3840 | FDA UDI | Class II | Unknown |
| CAMLOG® SCREW-LINE Implant, Promote® | K1044.4309 | FDA UDI | Class II | Unknown |
| Guide CAMLOG® SL Implant, Promote® plus | K1053.3811 | FDA UDI | Class II | Unknown |
| CAMLOG® SCREW-LINE Implant, Promote® | K1042.6013 | FDA UDI | Class II | Unknown |
| CAMLOG® Lab screw | J4004.2000 | FDA UDI | Class I | Active |
| CAMLOG® Ball abutment | J2250.4330 | FDA UDI | Class II | Unknown |
| CAMLOG® Vario SR abutment | K2560.5008 | FDA UDI | Class II | Unknown |
| CONELOG® Vario SR abutment | C2560.3808 | FDA UDI | Class II | Unknown |
| Guide CAMLOG® SL Implant, Promote® plus | K1053.3809 | FDA UDI | Class II | Unknown |
| Plaster cutter | J3706.3300 | FDA UDI | Class I | Active |
| CONELOG® SCREW-LINE Implant, Promote® plus | C1064.3309 | FDA UDI | Class II | Unknown |
| CAMLOG® Bar abutment | J2255.3820 | FDA UDI | Class II | Unknown |
| Reworking reamer | J3711.0025 | FDA UDI | Class I | Active |
| iSy® Implants-Set | P1110.3813 | FDA UDI | Class II | Active |
| iSy® Implants-Set | P1110.4413 | FDA UDI | Class II | Active |
| iSy® Lab analog | P3010.7010 | FDA UDI | Class I | Active |
| CONELOG® Healing cap, bottleneck | C2011.3340 | FDA UDI | Class II | Active |
| Guide CAMLOG® SL Implant, Promote® plus | K1053.3316 | FDA UDI | Class II | Unknown |
| CONELOG® Ball abutment set | C2250.3330 | FDA UDI | Class II | Unknown |
| Guide Template drill | J3713.4300 | FDA UDI | Class I | Active |
| CAMLOG® Healing Cap PS | K2004.5020 | FDA UDI | Class II | Unknown |
| Logfit® impression cap | J2551.6000 | FDA UDI | Class I | Active |
| iSy® Lab base | P3010.7020 | FDA UDI | Class I | Active |
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