Tapered Screw-Vent® Implant System

101 catalogue numbers from ZCRKIT4S, listed by ZimVie US Corp LLC, United States, under Abutment, Implant, Dental, Endosseous. 15 manufacturers in China are registered for this product code.

Registry build 21.09.26
15manufacturers in China registered for this device type
101catalogue 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 Tapered Screw-Vent® Implant System
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
510(k) K113092
Record published 2015-10-21
Record revised 2026-01-15 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2023-06-20
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Tapered Screw-Vent® Implant System
Catalogue number Size Status
ZCRKIT4S Ø4.5mm In distribution
ZCPROV5S Ø5.5mm In distribution
PT564S Ø5.7mm, Ø6.5mm x 4mm In distribution
SAPROV5 Ø5.5mm In distribution
ZRA451S Ø4.5mm, Ø5.5mm x 1mm In distribution
HC463 Ø4.5mm, Ø6.5mm x 3mm In distribution
ZRA461A Ø4.5mm, Ø6.0mm x 1mm In distribution
30AT424 Ø4.5mm, 2mm/4mm In distribution
PT344A Ø3.5mm, Ø4.5mm x 4mm In distribution
ZCRKIT5S Ø5.5mm In distribution
15AT434 Ø4.5mm, 3mm/4mm In distribution
SAPROVP5 Ø5.5mm In distribution
HC457 Ø4.5mm, Ø5.5mm x 7mm In distribution
ZRA351A Ø3.5mm, Ø5.0mm x 1mm In distribution
ZCPROV5A Ø5.5mm In distribution
ZCPROV4A Ø4.5mm In distribution
ZRA352A In distribution
DHTS2 In distribution
ZCPROV3A Ø3.5mm In distribution
TA5C4 Ø5.7mm, 4mm In distribution
ZCRKIT5A Ø5.5mm In distribution
30AT346 Ø3.5mm, 4mm/6mm In distribution
TA5C3 Ø5.7mm, 3mm In distribution
15AT323 Ø3.5mm, 2mm/3mm In distribution
TA5C1 Ø5.7mm, 0.75mm In distribution
TACW1 Ø4.5mm, 0.75mm In distribution
HC565 Ø5.7mm, Ø6.5mm x 5mm In distribution
30AT335 Ø3.5mm, 3mm/5mm In distribution
15AT423 Ø4.5mm, 2mm/3mm In distribution
PT454A Ø4.5mm; Ø5.5mm x 4mm In distribution
ZCRKIT3A Ø3.5mm In distribution
PSATH4RM Ø4.5mm In distribution
30AT446 Ø4.5mm, 4mm/6mm In distribution
HC563 Ø5.7mm, Ø6.5mm x 3mm In distribution
PT454S Ø4.5mm, Ø5.5mm x 4mm In distribution
ZCRKIT4A Ø4.5mm In distribution
30AT435 Ø4.5mm, 3mm/5mm In distribution
HC455 Ø4.5mm, Ø5.5mm x 5mm In distribution
PT341S Ø3.5mm, Ø4.5mm x 1mm In distribution
ZCPROV4S Ø4.5mm In distribution
PT341A Ø3.5mm, Ø4.5mm x 1mm In distribution
ZRA452S Ø4.5mm, Ø5.5mm x 2mm In distribution
30AT324 Ø3.5mm, 2mm/4mm In distribution
15AT312 Ø3.5mm, 1mm/2mm In distribution
ZRA341S Ø3.5mm, Ø4.5mm x 1mm In distribution
ZRA462A Ø4.5mm, Ø6.0mm x 2mm In distribution
15AT412 Ø4.5mm, 1mm/2mm In distribution
ZCRKIT6S Ø6.5mm In distribution
SAHEAL4 Ø4.5mm In distribution
SAHEAL6 Ø6.5mm In distribution
PT344S Ø3.5mm, Ø4.5mm x 4mm In distribution
SAPROVP4 Ø4.5mm In distribution
ZCRKIT6A Ø6.5mm In distribution
HC445 Ø4.5mm, Ø4.5mm x 5mm In distribution
TAC1 Ø3.5mm, 0.75mm In distribution
15AT334 Ø3.5mm, 3mm/4mm In distribution
HC465 Ø4.5mm, Ø6.5mm x 5mm In distribution
ZCPROV3S Ø3.5mm In distribution
ZCRKIT3S Ø3.5mm In distribution
PT451S Ø4.5mm, Ø5.5mm x 1mm In distribution
ZRA342S Ø3.5mm, Ø4.5mm x 2mm In distribution
PT451A Ø4.5mm, Ø5.5mm x 1mm In distribution
SAHEAL5 Ø5.5mm In distribution
SAPROVP6 Ø6.5mm In distribution
ZCPROV6A Ø6.5mm In distribution
TA5C2 Ø5.7mm, 2mm In distribution
ZCPROV6S Ø6.5mm In distribution
PT561S Ø5.7mm, Ø6.5mm x 1mm In distribution
PSAZH4L Ø4.5mm Withdrawn
ZOCPROV5S Ø5.5mm Withdrawn
ZOCHEAL4A Ø4.5mm Withdrawn
ZOCHEAL3A Ø3.5mm Withdrawn
ZOCPROV5A Ø5.5mm Withdrawn
PSAZH4 Ø4.5mm Withdrawn
ZOCHEAL6S Ø6.5mm Withdrawn
PSAZH3RM Ø3.5mm Withdrawn
PSAZH4RML Ø4.5mm Withdrawn
PSAZH4RFL Ø4.5mm Withdrawn
PSAZH4MRM Ø4.5mm Withdrawn
ZOCPROV3A Ø3.5mm Withdrawn
ZOCPROV4A Ø4.5mm Withdrawn
PSAZH3RML Ø3.5mm Withdrawn
ZOCHEAL5A Ø5.5mm Withdrawn
PSAZH3L Ø3.5mm Withdrawn
ZOCHEAL3S Ø3.5mm Withdrawn
PSATH5L Ø5.7mm Withdrawn
PSAZH3MRM Ø3.5mm Withdrawn
PSAZH3 Ø3.5mm Withdrawn
ZOCHEAL4S Ø4.5mm Withdrawn
PSAZH3M Ø3.5mm Withdrawn
ZOCPROV6A Ø6.5mm Withdrawn
ZOCHEAL6A Ø6.5mm Withdrawn
PSAZH3RFL Ø3.5mm Withdrawn
PSAZH4RM Ø4.5mm Withdrawn
SAPROV4 Ø4.5mm Withdrawn
ZOCPROV3S Ø3.5mm Withdrawn
ZOCHEAL5S Ø5.5mm Withdrawn
PSAZH4M Ø4.5mm Withdrawn
PSAZH4RF Ø4.5mm Withdrawn
SAPROV6 Ø6.5mm Withdrawn
PSAZH3RF Ø3.5mm Withdrawn

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

40 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 10 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 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 9 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 1 unit 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 4 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 35 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
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
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
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
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
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
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