Immediate Molar

Single Patient Immediate Molar Shaping Drill 5.4mmD, 11.5mmL

Registry build 21.09.26
70manufacturers in China registered for this device type
66catalogue numbers in this listing
14recalls on this code

Who Else Makes It

Concentrated in Guangdong (28), Jiangsu (9), Zhejiang (6). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NDP
Manufacturer City Province Registered as Device types
Shenzhen Denco Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 52
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
iBrite Suzhou Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 18
Digital Dental Depot Zhuhai Guangdong Contract manufacturer 17
Xiamen Yizhou IMP. & EXP. Co., Ltd. Xiamen Fujian Contract manufacturer 10
Amedcon Medical Technology (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 7
Ningbo Sezen Technology Co., Ltd. Ningbo Zhejiang Contract manufacturer 7
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Shanghai Jolly Industrial Co., Ltd. Shanghai Shanghai Contract manufacturer 99
Shanghai Lions Industrial Co., Ltd. Shanghai Shanghai Contract manufacturer 82
Wuxi Lyusmile IMP AND EXP Co., Ltd. Wuxi Jiangsu Private-label distributor 66

Showing 12 of 70. All 70 manufacturers in China registered for Accessories, Implant, Dental, Endosseous

Record

Regulatory record for Immediate Molar
Listed by ZimVie US Corp LLC, United States
FDA product code NDP
Device type Accessories, Implant, Dental, Endosseous
Device class Class 1
Regulation 21 CFR 872.3980
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2025-03-14
Record revised 2026-01-15 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Immediate Molar
Catalogue number Size Status
IMDIR38 In distribution
IMDR711 In distribution
IMDR98 In distribution
IMDR910 In distribution
IMDI9 In distribution
IMDR611 In distribution
IMDR910SP In distribution
IMDR34T3PSP In distribution
IMDR56SP In distribution
IMDI7 In distribution
IMDR511 In distribution
IMDR68 In distribution
IMDR51T3PSP In distribution
IMDR98SP In distribution
IMDIR34 In distribution
IMDR711SP In distribution
IMDR811 In distribution
IMDR610 In distribution
IMDR38TSXSP In distribution
IMDR66SP In distribution
IMDR76 In distribution
IMDR810SP In distribution
IMDR610SP In distribution
IMDR38T3P In distribution
IMDR28SSP In distribution
IMDR88SP In distribution
IMDR511SP In distribution
IMDR86 In distribution
IMDR911 In distribution
IMDR811SP In distribution
IMDR68SP In distribution
IMDR56 In distribution
IMDR58 In distribution
IMDI8 In distribution
IMDIR44 In distribution
IMDIR51 In distribution
IMDR44T3P In distribution
IMDR28L In distribution
IMDR58SP In distribution
IMDR38T3PSP In distribution
IMDR510 In distribution
IMDR710SP In distribution
IMDI6 In distribution
IMDR28LSP In distribution
IMDR96 In distribution
IMDR911SP In distribution
IMDR66 In distribution
IMDR34TSX In distribution
IMDR76SP In distribution
IMDR34TSXSP In distribution
IMDR28S In distribution
IMDR510SP In distribution
IMDR86SP In distribution
IMDR78SP In distribution
IMDR710 In distribution
IMDR88 In distribution
IMDR44TSXSP In distribution
IMDR44T3PSP In distribution
IMDR34T3P In distribution
IMDR96SP In distribution
IMDR78 In distribution
IMDR611SP In distribution
IMDR38TSX In distribution
IMDR44TSX In distribution
IMDR51T3P In distribution
IMDR810 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Accessories, Implant, Dental, Endosseous Southern Implants (PTY) Ltd 1,379
Accessories, Implant, Dental, Endosseous Institut Straumann AG 1,320
Neobiotech Implant System Neobiotech Co., Ltd. 1,112
Inclusive Prismatik Dentalcraft, Inc. 1,045
Medentika Medentika GmbH 1,042
BioHorizons Biohorizons Implant Systems Inc. 1,008
IPD Implant Protesis Dental 2004 SL 998
Klockner Soadco, S.L. 995
Dynamic Abutment Solutions Talladium España, SL 877
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 738
Nobel Biocare® Nobel Biocare AB 703
MIS MIS Implants Technologies Ltd. 615

Showing 12 of 7,548. All products under Accessories, Implant, Dental, Endosseous

Recalls

14 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
2017-10-11 Class II Employee error The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. 356 units 2019-03-13
2017-10-11 Class II Employee error The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. 891 kits 2019-03-13
2017-10-11 Class II Employee error The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. 166 kits 2019-03-13
2017-10-11 Class II Employee error The device may contain a manufacturing condition affecting the geometry of the driver’s hex feature which prevents it from properly engaging the fixture mount transfer and/or a dental implant. 30 kits 2019-03-13
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. 76 products 2019-08-05
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. 86 products 2019-08-05
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. 423 products 2019-08-05
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. 349 products 2019-08-05
2015-11-16 Class II Software design (manufacturing process) Images contained within radiographic transparency ART 1036 are undersized. 686 2016-12-14
2015-09-21 Class II Process control Inadequate biocompatibility testing. 30,111 devices. 2016-10-12
2015-09-21 Class II Process control Inadequate biocompatibility testing. 30,111 devices. 2016-10-12
2015-08-10 Class II Labeling mix-ups RASQ3N, a square, abutment screw driver tip has been labeled and distributed as RASH3N, a hexed, abutment screw driver tip. Additionally, the RASQ3N received the RASH3N’s laser marking “RASH3N” during manufacturing. 103 pieces 2016-10-12
2015-08-10 Class II Labeling mix-ups The RASH3N, a hexed, abutment screw driver tip has been labeled and distributed as RASQ3N, a square, abutment screw driver tip. Additionally, the RASQ3N received the RASH3N’s laser marking “RASH3N” during manufacturing. 96 pieces 2016-10-12
2015-01-22 Class II Device Design The Gemlock Long Hex Driver may not fit into the Fixture Mount Transfer (FMT) or the internal hex of the implant. 627 units 2015-08-03

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