Certain® Bellatek®

Certain® Bellatek® Titanium Abutment 5.0MM

Registry build 21.09.26
15manufacturers in China registered for this device type
40catalogue numbers in this listing
40recalls on this code

Who Else Makes It

Concentrated in Guangdong (11), Jiangsu (2), Shanghai (1). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NHA
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Modern Dental Laboratory (DG) Co., Ltd. Dongguan Guangdong Contract manufacturer 15
Exceldent Dental Technology Development Co., Ltd. Zhuhai Guangdong Contract manufacturer 12
DTS Digital Dental LAB Shenzhen Guangdong Contract manufacturer 11
KTJ Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Shimmer Computerized Dental Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 10
Zhuhai Crystal Dental Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 9
NEW Perfect Dental LAB Shenzhen Guangdong Contract manufacturer 8
Shenzhen Jiahong Dental Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 7
Jiangsu Trausim Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
Chengdu Besmile Medical Technology Co., Ltd. Chengdu Sichuan Manufacturer 14
CBD Dental LAB, Inc Shenzhen Guangdong Manufacturer 11

Showing 12 of 15. All 15 manufacturers in China registered for Abutment, Implant, Dental, Endosseous

Record

Regulatory record for Certain® Bellatek®
Listed by ZimVie US Corp LLC, United States
FDA product code NHA
Device type Abutment, Implant, Dental, Endosseous
Device class Class 2
Regulation 21 CFR 872.3630
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-09-03
Record revised 2026-01-15 (version 7)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Certain® Bellatek®
Catalogue number Size Status
IIAN3 Diameter 3.4 mm In distribution
ISAT5 Diameter 5 mm In distribution
IEDAN3 Diameter 3.4 mm In distribution
ISAN5 Diameter 5 mm In distribution
ISAN6 Diameter 6 mm In distribution
IIAT5 Diameter 5 mm In distribution
IIAN4 Diameter 4.1 mm In distribution
IEDAT5 Diameter 5 mm In distribution
ILDAT6 Diameter 6 mm In distribution
ILDAN5 Diameter 5 mm In distribution
IEDAN5 Diameter 5 mm In distribution
IEDAT3 Diameter 3.4 mm In distribution
I3MAT5 Diameter 5 mm In distribution
ILDAT3 Diameter 3.4 mm In distribution
I3MAN6 Diameter 6 mm In distribution
ILDAN6 Diameter 6 mm In distribution
ISAN4 Diameter 4.1 mm In distribution
I3MAT3 Diameter 3.4 mm In distribution
I3MAT4 Diameter 4.1 mm In distribution
ISAT3 Diameter 3.4 mm In distribution
ISAT4 Diameter 4.1 mm In distribution
I3MAN4 Diameter 4 mm In distribution
IEDAN4 Diameter 4.1 mm In distribution
IIAN6 Diameter 6 mm In distribution
IIAT6 Diameter 6 mm In distribution
ISAT6 Diameter 6 mm In distribution
ISAN3 Diameter 3.4 mm In distribution
IEDAN6 Diameter 6 mm In distribution
IIAT3 Diameter 3.4 mm In distribution
IIAT4 Diameter 4.1 mm In distribution
ILDAN4 Diameter 4.1 mm In distribution
ILDAT5 Diameter 5 mm In distribution
ILDAN3 Diameter 3.4 mm In distribution
IEDAT6 Diameter 6 mm In distribution
ILDAT4 Diameter 4.1 mm In distribution
IEDAT4 Diameter 4.1 mm In distribution
I3MAN3 Diameter 3.4 mm In distribution
IIAN5 Diameter 5 mm In distribution
I3MAN5 Diameter 5 mm In distribution
I3MAT6 Diameter 6 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
MEDENTiKA Medentika GmbH 2,553
LW Vis Abutment Ossvis Co., Ltd. 2,520
Dess dental smart solutions Terrats Medical SL 1,715
Locator Zest Anchors, LLC 1,643
NobelProcera® Nobel Biocare AB 1,526
Azure Terrats Medical SL 1,360
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 1,308
LW Vis Abutment SET Ossvis Co., Ltd. 1,260
Abutment, Implant, Dental, Endosseous Southern Implants (PTY) Ltd 1,240
Healing Abutment Megagen Implant Co., Ltd. 1,218
Chaorum Implant System Medimecca Co Ltd 1,084
OT Equator Rhein 83 SRL 1,051

Showing 12 of 6,204. All products under Abutment, Implant, Dental, Endosseous

Recalls Naming This Product

10 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Certain® Bellatek®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
ZimVie US Corp LLC UDI-DI 2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 9 units 2022-07-06
ZimVie US Corp LLC UDI-DI 2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 4 units 2022-07-06
ZimVie US Corp LLC UDI-DI 2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 35 units 2022-07-06
ZimVie US Corp LLC UDI-DI 2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 10 units 2022-07-06
ZimVie US Corp LLC UDI-DI 2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 1 unit 2022-07-06
ZimVie US Corp LLC UDI-DI 2019-02-26 Class II Process control During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop. 3 units 2020-06-15
ZimVie US Corp LLC UDI-DI 2019-02-26 Class II Process control During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop. 17 units 2020-06-15
ZimVie US Corp LLC UDI-DI 2019-02-26 Class II Process control During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop. 6 units 2020-06-15
ZimVie US Corp LLC UDI-DI 2019-02-26 Class II Process control During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop. 2 units 2020-06-15
ZimVie US Corp LLC UDI-DI 2019-02-26 Class II Process control During manufacturing, the screw stop ledge was not made to specification and location within the abutment, resulting in the screw head seating deeper in the abutment with no positive stop. 49 units 2020-06-15

Recalls

30 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 7 stand alone units 2022-07-06
2020-08-31 Class II Device Design Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientati 2 units 2022-07-06
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2020-01-10 Class II Process control Resulting impression or scanned data produced from the Healing Abutment lots will result in an incorrect rotation of approximately 30 degrees and/or margin contour misalignment 2021-08-02
2016-09-14 Class II Employee error A limited number of product pouches may not have been sealed during packaging. 525 2019-07-26
2016-09-14 Class II Employee error A limited number of product pouches may not have been sealed during packaging. 108 2019-07-26
2016-09-14 Class II Employee error A limited number of product pouches may not have been sealed during packaging. 735 2019-07-26
2016-09-14 Class II Employee error A limited number of product pouches may not have been sealed during packaging. 123 2019-07-26
2016-09-14 Class II Employee error A limited number of product pouches may not have been sealed during packaging. 160 2019-07-26

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer