Not currently registered with FDA under this name
Nobel Biocare Uas, Inc.
Yorba Linda,, CA, United States. Named as applicant on 31 dental 510(k) clearances between 1997 and 2005. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 311997–2005
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Nobel Biocare Uas, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 7 Jul 2005 | K050444 | NOBELREPLACE ADAPTER, MODEL 32412 | NHA Endosseous Dental Implant Abutment |
| 20 Oct 2004 | K042658 | PROCERA ABUTMENT BRANEMARK, MODELS 10-4001, 10-4004, 10-5001, 10-5004, 10-6001, 10-6004 | NHA Endosseous Dental Implant Abutment |
| 26 Aug 2004 | K041661 | NOBEL BIOCARE ENDOSSEOUS IMPLANTS | DZE Root-Form Endosseous Implant |
| 20 Aug 2004 | K041876 | NOBELDIRECT OD IMPLANT | DZE Root-Form Endosseous Implant |
| 23 Jul 2004 | K041312 | NOBELRONDO DENTAL CERAMIC-ALUMINA | EIH Porcelain Powder |
| 27 May 2004 | K041275 | PROCERA ABUTMENT OCTAGON | NHA Endosseous Dental Implant Abutment |
| 28 Apr 2004 | K040573 | NOBEL BIOCARE PERMANENT CENTRIC POST, MODELS 31234, 31235, 31236 | NHA Endosseous Dental Implant Abutment |
| 23 Feb 2004 | K033724 | NOBEL BIOCARE CENTRIC POST, MODELS 31234, 31235 AND 31236 | NHA Endosseous Dental Implant Abutment |
| 24 Jul 2003 | K031345 | NOBEL DIRECT, MODELS 30937, 30938 | DZE Root-Form Endosseous Implant |
| 10 Feb 2003 | K030257 | NOBEL PERFECT IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 16 Jan 2003 | K023952 | REPLACE ONE PIECE IMPLANT, HA, REPLACE ONE PIECE IMPLANT, TIUNITE | DZE Root-Form Endosseous Implant |
| 27 Sep 2002 | K022424 | REPLACE HA COATED IMPLANT, MODELS 35102, 35132, 35162, 43102, 43132, 43162, 50102, 50132, 50162, 60102, 60132 & 60162 | DZE Root-Form Endosseous Implant |
| 26 Sep 2002 | K023113 | REPLACE TIUNITE ENDOSSEOUS IMPLANT | DZE Root-Form Endosseous Implant |
| 5 Jun 2002 | K021584 | REPLACE SCALLOPED MARGIN IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 29 May 2002 | K020646 | REPLACE HA COATED IMPLANT, MODELS 35102, 35132, 35162, 43102, 43132, 43162, 50102, 50132, 50162, 60102, 60132, & 60162 | DZE Root-Form Endosseous Implant |
| 9 Nov 2000 | K002475 | REPLACE TPS COATED IMPLANTS | DZE Root-Form Endosseous Implant |
| 7 Sep 2000 | K000643 | INPLANT ORTHODONTIC ANCHOR SYSTEM | DZE Root-Form Endosseous Implant |
| 30 Mar 2000 | K000018 | BRANEMARK NOVUM | DZE Root-Form Endosseous Implant |
| 29 Feb 2000 | K992937 | DENTAL IMPLANT | DZE Root-Form Endosseous Implant |
| 28 Jan 2000 | K993595 | NOBEL BIOCARE'S MODIFIED SURFACE IMPLANT (INTENDED FOR IMMEDIATE LOADING UPON PLACEMENT) | DZE Root-Form Endosseous Implant |
| 23 Nov 1999 | K992538 | AMORPHOUS DIAMOND COATED SCREW | DZE Root-Form Endosseous Implant |
| 10 Jun 1999 | K990846 | AMORPHOUS DIAMOND COATED DRILL | DZI Powered Bone Drill |
| 1 Mar 1999 | K984287 | PROVISIONAL DENTAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 18 Nov 1998 | K983453 | PROCERA ALLCERAM FUSING MATERIAL | EIH Porcelain Powder |
| 26 May 1998 | K974123 | BRANEMARK SYSTEM DEC 600 DRILLING UNIT | DZE Root-Form Endosseous Implant |
| 5 May 1998 | K980460 | ONPLANT ORTHODONTIC SYSTEM | DZE Root-Form Endosseous Implant |
| 24 Mar 1998 | K974828 | BRANEMARK SYSTEM(R) EBON(TM) FIXTURE | DZE Root-Form Endosseous Implant |
| 23 Jan 1998 | K974150 | PROCERA PREPARABLE ABUTMENT SYSTEM | NHA Endosseous Dental Implant Abutment |
| 16 Oct 1997 | K970499 | BRANEMARK SYSTEM ZYGOMATICUS FIXTURE SYSTEM | DZE Root-Form Endosseous Implant |
| 12 Sep 1997 | K972475 | AURADAPT AUBTMENT SYSTEM | NHA Endosseous Dental Implant Abutment |
| 21 Jul 1997 | K971706 | TIADAPT ABUTMENT SYSTEM | NHA Endosseous Dental Implant Abutment |
Some of these clearances are listed with FDA today by another company: Nobel Biocare Services AG (7), Topway Dental Laboratory Co., Ltd (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.