Is this your brand? Sign in to claim ownership.
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 10 of 43| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CONELOG® Esthomic® abutment | C2228.3330 | FDA UDI | Class II | Unknown |
| Screwdriver Activator for Matrix CM Dalbo®-Plus | J5315.0005 | FDA UDI | Class I | Active |
| Guide System Starter Set, PL | J5300.0074 | FDA UDI | Class I | Active |
| CONELOG® collet | C3720.5000 | FDA UDI | Class I | Active |
| CONELOG® SCREW-LINE Implant, Promote® plus | C1062.3811 | FDA UDI | Class II | Unknown |
| CAMLOG® Ceramic abutment | K2242.3840 | FDA UDI | Class II | Unknown |
| CONELOG® Ball abutment set | C2250.3315 | FDA UDI | Class II | Unknown |
| CAMLOG® SCREW-LINE Implant, Promote® | K1042.3813 | FDA UDI | Class II | Unknown |
| CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus | K1076.3316 | FDA UDI | Class II | Active |
| CONELOG® Vario SR abutment | C2561.5000 | FDA UDI | Class II | Unknown |
| iSy® Implants-Set | P1210.4413 | FDA UDI | Class II | Unknown |
| Vario SR plastic coping | J2563.4301 | FDA UDI | Class I | Active |
| CONELOG® Logfit® abutment | C2550.5025 | FDA UDI | Class II | Unknown |
| Guide CONELOG® Insertion post | C2026.3803 | FDA UDI | Class I | Active |
| CONELOG® Ball abutment set | C2250.3830 | FDA UDI | Class II | Unknown |
| CAMLOG® SCREW-LINE Implant, Promote® | K1044.3813 | FDA UDI | Class II | Unknown |
| CAMLOG® Impression post | K2119.4300 | FDA UDI | Class I | Active |
| CAMLOG® SCREW-LINE Implant, Promote® | K1044.4311 | FDA UDI | Class II | Unknown |
| CONELOG® Vario SR abutment | C2560.4308 | FDA UDI | Class II | Unknown |
| Vario SR analog | J2567.6000 | FDA UDI | Class I | Active |
| Guide CONELOG® SL Implant, Promote® plus | C1063.4307 | FDA UDI | Class II | Unknown |
| Base for CONELOG® Bar abutment | C2263.4300 | FDA UDI | Class II | Unknown |
| Surgery set, PL | J5300.0065 | FDA UDI | Class I | Active |
| Guide Template drill | J3713.3300 | FDA UDI | Class I | Active |
| Logfit® analog | J2552.6000 | FDA UDI | Class I | Active |
| CONELOG® Bar abutment | C2255.3810 | FDA UDI | Class II | Unknown |
| CAMLOG® SCREW-LINE Implant, Promote® plus | K1052.6011 | FDA UDI | Class II | Unknown |
| CONELOG® Esthomic® abutment | C2226.3330 | FDA UDI | Class II | Active |
| CAMLOG® Logfit® abutment | K2550.5008 | FDA UDI | Class II | Active |
| CAMLOG® Bar abutment | J2255.6040 | FDA UDI | Class II | Unknown |
| CAMLOG® Ball abutment | J2250.3815 | FDA UDI | Class II | Active |
| CAMLOG® SCREW-LINE Implant, Promote® plus | K1052.6016 | FDA UDI | Class II | Unknown |
| iSy® Implants-Set | P1110.5007 | FDA UDI | Class II | Active |
| CAMLOG® SCREW-LINE Implant, Promote® plus | K1054.6013 | FDA UDI | Class II | Unknown |
| CAMLOG® Bar abutment | J2255.5040 | FDA UDI | Class II | Unknown |
| CAMLOG® CAM Titanium Blank, type IAC | K2411.3813 | FDA UDI | Class II | Active |
| Guide CAMLOG® SL Implant, Promote® plus | K1053.4311 | FDA UDI | Class II | Unknown |
| Guide Check-up pin | J5301.3300 | FDA UDI | Class I | Active |
| CONELOG® Lab screw | C4004.1600 | FDA UDI | Class I | Active |
| CAMLOG® Vario SR abutment | K2560.4308 | FDA UDI | Class II | Unknown |
| Removal adapter, CAMLOG® | K5302.4301 | FDA UDI | Class I | Active |
| CAMLOG® SCREW-LINE Implant, Promote® | K1044.3316 | FDA UDI | Class II | Unknown |
| Healing cap for CONELOG® Bar abutment | C2030.4300 | FDA UDI | Class II | Active |
| Collet | J3709.6000 | FDA UDI | Class I | Active |
| CONELOG® Logfit® abutment | C2550.3825 | FDA UDI | Class II | Unknown |
| Guide CAMLOG® SL Implant, Promote® plus | K1053.3311 | FDA UDI | Class II | Unknown |
| CONELOG® SCREW-LINE Implant, Promote® plus | C1064.5007 | FDA UDI | Class II | Unknown |
| Removal adapter, CAMLOG® | K5302.6001 | FDA UDI | Class I | Unknown |
| Zirconium oxide sleeve, for CAMLOG® ceramic abutment | J2242.4341 | FDA UDI | Class II | Unknown |
| Titanium bonding base for CAMLOG® bar abutment | J2260.4300 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.