Tapered Screw-Vent

124 catalogue numbers from TSV4B11, listed by ZimVie US Corp LLC, United States, under Implant, Endosseous, Root-Form. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
124catalogue numbers in this listing
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Sichuan (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZE
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Jiangsu Trausim Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
Basic (Chengdu) Medical Device Co., Ltd. Chengdu Sichuan Contract manufacturer 1
Dongguan Xinlonghong Hardware Co., Ltd. Dongguan Guangdong Contract manufacturer 1
Chengdu Besmile Medical Technology Co., Ltd. Chengdu Sichuan Manufacturer 14
BIO Concept Co., Ltd. Changzhou Jiangsu Manufacturer 5

Record

Regulatory record for Tapered Screw-Vent
Listed by ZimVie US Corp LLC, United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K133339
Record published 2015-09-24
Record revised 2026-01-15 (version 7)

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
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Tapered Screw-Vent
Catalogue number Size Status
TSV4B11 Ø4.1mm x 11.5mm, Ø3.5mm In distribution
TSV4B13 Ø4.1mm x 13mm, Ø3.5mm In distribution
TSVH11 Ø3.7mm x 11.5mm, Ø3.5mm In distribution
TSVT6H13 Ø6.0mm x 13mm, Ø5.7mm In distribution
TSVT6B16 Ø6.0mm x 16mm, Ø5.7mm In distribution
TSVTWB16 Ø4.7mm x 16mm, Ø4.5mm In distribution
TSVMH10 Ø3.7mm x 10mm, Ø3.5mm In distribution
TSVMWH13 Ø4.7mm x 13mm, Ø4.5mm In distribution
TSVTH8 Ø3.7mm x 8mm, Ø3.5mm In distribution
TSVTH11 Ø3.7mm x 11.5mm, Ø3.5mm In distribution
TSVB13 Ø3.7mm x 13mm, Ø3.5mm In distribution
TSV6H10 Ø6.0mm x 10mm, Ø5.7mm In distribution
TSVTWH10 Ø4.7mm x 10mm, Ø4.5mm In distribution
TSVTB11 Ø3.7mm x 11.5mm, Ø3.5mm In distribution
TSV6B10 Ø6.0mm x 10mm, Ø5.7mm In distribution
TSVM4B10 Ø4.1mm x 10mm, Ø3.5mm In distribution
TSVWH16 Ø4.7mm x 16mm, Ø4.5mm In distribution
TSVMB10 Ø3.7mm x 10mm, Ø3.5mm In distribution
TSV4B10 Ø4.1mm x 10mm, Ø3.5mm In distribution
TSVTWH8 Ø4.7mm x 8mm, Ø4.5mm In distribution
TSVTWH13 Ø4.7mm x 13mm, Ø4.5mm In distribution
TSVB11 Ø3.7mm x 11.5mm, Ø3.5mm In distribution
TSV4H10 Ø4.1mm x 10mm, Ø3.5mm In distribution
TSVT4B8 Ø4.1mm x 8mm, Ø3.5mm In distribution
TSV6H11 Ø6.0mm x 11.5mm, Ø5.7mm In distribution
HLPT4 Ø4.5mm, Ø5.5mm x 1mm In distribution
TSV6B11 Ø6.0mm x 11.5mm, Ø5.7mm In distribution
TSVMH13 Ø3.7mm x 13mm, Ø3.5mm In distribution
TSVM6B11 Ø6.0mm x 11.5mm, Ø5.7mm In distribution
TSVT4B11 Ø4.1mm x 11.5mm, Ø3.5mm In distribution
TSVTB13 Ø3.7mm x 13mm, Ø3.5mm In distribution
TSVWB10 Ø4.7mm x 10mm, Ø4.5mm In distribution
TSVMWB16 Ø4.7mm x 16mm, Ø4.5mm In distribution
TSVT4B16 Ø4.1mm x 16mm, Ø3.5mm In distribution
TSVMB11 Ø3.7mm x 11.5mm, Ø3.5mm In distribution
TSVWB13 Ø4.7mm x 13mm, Ø4.5mm In distribution
HLPT5 Ø5.7mm, Ø6.5mm x 1mm In distribution
TSV4H13 Ø4.1mm x 13mm, Ø3.5mm In distribution
TSVM6B16 Ø6.0mm x 16mm, Ø5.7mm In distribution
TSVMWH11 Ø4.7mm x 11.5mm, Ø4.5mm In distribution
TSVH16 Ø3.7mm x 16mm, Ø3.5mm In distribution
TSVTWB10 Ø4.7mm x 10mm, Ø4.5mm In distribution
TSVMH8 Ø3.7mm x 8mm, Ø3.5mm In distribution
TSVTB8 Ø3.7mm x 8mm, Ø3.5mm In distribution
TSVTB16 Ø3.7mm x 16mm, Ø3.5mm In distribution
TSVTWB8 Ø4.7mm x 8mm, Ø4.5mm In distribution
TSV6H16 Ø6.0mm x 16mm, Ø5.7mm In distribution
TSVM4B13 Ø4.1mm x 13mm, Ø3.5mm In distribution
TSVMH16 Ø3.7mm x 16mm, Ø3.5mm In distribution
TSV6B13 Ø6.0mm x 13mm, Ø5.7mm In distribution
TSVB8 Ø3.7mm x 8mm, Ø3.5mm In distribution
TSVT6B11 Ø6.0mm x 11.5mm, Ø5.7mm In distribution
TSVMWB11 Ø4.7mm x 11.5mm, Ø4.5mm In distribution
TSV4H8 Ø4.1mm x 8mm, Ø3.5mm In distribution
TSVM4B11 Ø4.1mm x 11.5mm, Ø3.5mm In distribution
TSVH8 Ø3.7mm x 8mm, Ø3.5mm In distribution
TSVMB16 Ø3.7mm x 16mm, Ø3.5mm In distribution
TSVTB10 Ø3.7mm x 10mm, Ø3.5mm In distribution
TSVM6H11 Ø6.0mm x 11.5mm, Ø5.7mm In distribution
TSVMWB10 Ø4.7mm x 10mm, Ø4.5mm In distribution
TSVM4B16 Ø4.1mm x 16mm, Ø3.5mm In distribution
TSVT6H16 Ø6.0mm x 16mm, Ø5.7mm In distribution
TSVMWH10 Ø4.7mm x 10mm, Ø4.5mm In distribution
TSVM4H11 Ø4.1mm x 11.5mm, Ø3.5mm In distribution
TSVWB16 Ø4.7mm x 16mm, Ø4.5mm In distribution
TSV4B16 Ø4.1mm x 16mm, Ø3.5mm In distribution
TSVWB8 Ø4.7mm x 8mm, Ø4.5mm In distribution
TSVT4B10 Ø4.1mm x 10mm, Ø3.5mm In distribution
TSVWH8 Ø4.7mm x 8mm, Ø4.5mm In distribution
TSV4B8 Ø4.1mm x 8mm, Ø3.5mm In distribution
TSVMB13 Ø3.7mm x 13mm, Ø3.5mm In distribution
TSVTWH11 Ø4.7mm x 11.5mm, Ø4.5mm In distribution
TSVT4H10 Ø4.1mm x 10mm, Ø3.5mm In distribution
TSVT6B13 Ø6.0mm x 13mm, Ø5.7mm In distribution
TSVH10 Ø3.7mm x 10mm, Ø3.5mm In distribution
TSVB10 Ø3.7mm x 10mm, Ø3.5mm In distribution
TSVT4H16 Ø4.1mm x 16mm, Ø3.5mm In distribution
TSV4H11 Ø4.1mm x 11.5mm, Ø3.5mm In distribution
TSV6H8 Ø6.0mm x 8mm, Ø5.7mm In distribution
TSVM4H10 Ø4.1mm x 10mm, Ø3.5mm In distribution
TSVTH10 Ø3.7mm x 10mm, Ø3.5mm In distribution
TSVM4H8 Ø4.1mm x 8mm, Ø3.5mm In distribution
TSVM4B8 Ø4.1mm x 8mm, Ø3.5mm In distribution
TSVM6H8 Ø6.0mm x 8mm, Ø5.7mm In distribution
PSATH4M Ø4.5mm In distribution
TSVB16 Ø3.7mm x 16mm, Ø3.5mm In distribution
TSVT6H10 Ø6.0mm x 10mm, Ø5.7mm In distribution
TSVT4H8 Ø4.1mm x 8mm, Ø3.5mm In distribution
TSVWH13 Ø4.7mm x 13mm, Ø4.5mm In distribution
TSVWH11 Ø4.7mm x 11.5mm, Ø4.5mm In distribution
TSVMWH16 Ø4.7mm x 16mm, Ø4.5mm In distribution
TSVTH16 Ø3.7mm x 16mm, Ø3.5mm In distribution
TSVTWB13 Ø4.7mm x 13mm, Ø4.5mm In distribution
TSVT6B8 Ø6.0mm x 8mm, Ø5.7mm In distribution
TSVMWH8 Ø4.7mm x 8mm, Ø4.5mm In distribution
TSVTH13 Ø3.7mm x 13mm, Ø3.5mm In distribution
TSVM6B13 Ø6.0mm x 13mm, Ø5.7mm In distribution
TSVH13 Ø3.7mm x 13mm, Ø3.5mm In distribution
TSV6H13 Ø6.0mm x 13mm, Ø5.7mm In distribution
TSVMWB13 Ø4.7mm x 13mm, Ø4.5mm In distribution
HLPT3 Ø3.5mm, Ø4.5mm x 1mm In distribution
TSVT4H13 Ø4.1mm x 13mm, Ø3.5mm In distribution
TSVT6H11 Ø6.0mm x 11.5mm, Ø5.7mm In distribution
TSVM6H10 Ø6.0mm x 10mm, Ø5.7mm In distribution
TSVTWH16 Ø4.7mm x 16mm, Ø4.5mm In distribution
TSVM6H16 Ø6.0mm x 16mm, Ø5.7mm In distribution
TSVM6B10 Ø6.0mm x 10mm, Ø5.7mm In distribution
TSV6B8 Ø6.0mm x 8mm, Ø5.7mm In distribution
TSVMWB8 Ø4.7mm x 8mm, Ø4.5mm In distribution
TSVT6H8 Ø6.0mm x 8mm, Ø5.7mm In distribution
TSVT6B10 Ø6.0mm x 10mm, Ø5.7mm In distribution
TSV4H16 Ø4.1mm x 16mm, Ø3.5mm In distribution
TSVMH11 Ø3.7mm x 11.5mm, Ø3.5mm In distribution
TSVTWB11 Ø4.7mm x 11.5mm, Ø4.5mm In distribution
TSV6B16 Ø6.0mm x 16mm, Ø5.7mm In distribution
TSVM4H16 Ø4.1mm x 16mm, Ø3.5mm In distribution
TSVWB11 Ø4.7mm x 11.5mm, Ø4.5mm In distribution
TSVT4H11 Ø4.1mm x 11.5mm, Ø3.5mm In distribution
TSVM6B8 Ø6.0mm x 8mm, Ø5.7mm In distribution
TSVM4H13 Ø4.1mm x 13mm, Ø3.5mm In distribution
TSVWH10 Ø4.7mm x 10mm, Ø4.5mm In distribution
TSVMB8 Ø3.7mm x 8mm, Ø3.5mm In distribution
TSVM6H13 Ø6.0mm x 13mm, Ø5.7mm In distribution
TSVT4B13 Ø4.1mm x 13mm, Ø3.5mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 920
Osstem Implant System Osstem Implant Co., Ltd. 788
Magicore InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) 744
Implant, Endosseous, Root-Form Southern Implants (PTY) Ltd 608
ITL Dental Emery Enterprises Inc. 603
Magicore S InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) 560
Friadent® Dentsply Implants Manufacturing GmbH 525
Sphero Block Normo Rhein 83 SRL 489
Neobiotech Implant System Neobiotech Co., Ltd. 483
KJ Mini Implant System Kjmeditech.co., Ltd. 448
Ritter Dental Implant System Ritter Implants GmbH & Co. KG 418
Leone SPA Leone SPA 404

Showing 12 of 2,762. All products under Implant, Endosseous, Root-Form

Recalls Naming This Product

7 recalls name this product by its own identifiers, the UDI on its label or the 510(k) it is cleared under.

Recalls naming the identifiers of Tapered Screw-Vent
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
ZimVie US Corp LLC UDI-DI 2018-05-10 Class II Labeling mix-ups Dental implants have incorrect item/lot numbers and size on the inner package labeling. Correct item/lot numbers and size are on the outer package labeling. 299 units 2020-08-19
ZimVie US Corp LLC UDI-DI 2017-11-29 Class II Packaging process control Two lots of the Tapered Screw-Vent Implants, with different outer thread diameters, were inadvertently commingled during the manufacturing process and may be mislabeled. 995 distribution events total 2019-02-08
ZimVie US Corp LLC UDI-DI 2017-11-29 Class II Packaging process control Two lots of the Tapered Screw-Vent Implants, with different outer thread diameters, were inadvertently commingled during the manufacturing process and may be mislabeled. 995 distribution events total 2019-02-08
ZimVie US Corp LLC UDI-DI 2017-11-20 Class II Under Investigation by firm Some implant vial caps in the recalled implant lot may inadvertently crack as the result of a manufacturing assembly condition. 500 units 2024-02-28
ZimVie US Corp LLC 510(k) number 2017-07-10 Class II Under Investigation by firm Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs. 13,235 products 2019-08-05
Zimmer, Inc. 510(k) number 2014-07-17 Class II Process design Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner vial state “03.7 x 8mm” instead of “04.7 x 8 mm.” 291 units 2015-02-06
Zimmer, Inc. 510(k) number 2009-11-06 Not classified Process control The devices may not meet specifications, which may result in fracturing during tightening of the component. 738 2010-10-08

Recalls

35 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
2017-07-10 Class II Under Investigation by firm Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs. 169 products 2019-08-05
2017-03-20 Class II Nonconforming Material/Component It was manufactured with the minor diameter of the internal thread that is below specification. 188 units 2017-11-01
2017-03-08 Class II Under Investigation by firm A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier 5 2019-08-02
2016-08-08 Class II Packaging process control Product was incorrectly packaged. 92 units 2019-08-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1050 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1050 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2016-01-06 Class II Labeling Change Control Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer Dental Implants was omitted from the latest revision of the applicable IFU in the Indications, Contraindications, and Precautions sections. 1059 2016-05-06
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to these recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to these recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to thIs recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to these recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1, 648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to these recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to these recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 (all products subject to these recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1, 648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26
2015-11-25 Class II Packaging Pouches may not have been sealed during packing. 1,648,273 devices (all products subject to this recall) 2019-07-26

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P800035 2001-10-04 PERI-OSS Curasan AG
P860012 1988-10-28 ALVEOFORM TM BIOGRAFT Collagen Corp.

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