Glidewell IH™

Glidewell IH™ Multi-Unit Coping 4.5 mmH, Non-Engaging, with Prosthetic Screw .050" Hex

Registry build 21.09.26
15manufacturers in China registered for this device type
77catalogue numbers in this listing
19510(k) clearances naming this product code
1recall

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 Glidewell IH™
Listed by Prismatik Dentalcraft, Inc., 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
510(k) K153099
Record published 2025-06-19
Record revised 2026-03-26 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Glidewell IH™
Catalogue number Size Status
70-1074-PRS0094 In distribution
70-1074-PRS0105 In distribution
70-1207-IMP0019 In distribution
70-1073-PRA0112 In distribution
70-1073-PRA0138 In distribution
70-1074-PRS0093 In distribution
70-1074-PRS0083 In distribution
70-1073-PRA0096 In distribution
70-1073-PRA0098 In distribution
70-1073-PRA0124 In distribution
70-1073-PRA0122 In distribution
70-1073-PRA0116 In distribution
70-1073-PRA0110 In distribution
70-1073-PRA0095 In distribution
70-1073-PRA0097 In distribution
70-1073-PRA0105 In distribution
70-1074-PRS0076 In distribution
70-1207-IMP0011 In distribution
70-1073-PRA0106 In distribution
70-1073-PRA0115 In distribution
70-1207-IMP0015 In distribution
70-1073-PRA0118 In distribution
70-1074-PRS0088 In distribution
70-1073-PRA0114 In distribution
70-1074-PRS0081 In distribution
70-1073-PRA0117 In distribution
70-1073-PRA0121 In distribution
70-1207-IMP0006 In distribution
70-1207-IMP0005 In distribution
70-1207-IMP0010 In distribution
70-1207-IMP0003 In distribution
70-1207-IMP0016 In distribution
70-1207-IMP0014 In distribution
70-1073-PRA0102 In distribution
70-1074-PRS0091 In distribution
70-1074-PRS0084 In distribution
70-1207-IMP0008 In distribution
70-1072-PRC0086 In distribution
70-1074-PRS0082 In distribution
70-1073-PRA0113 In distribution
70-1073-PRA0101 In distribution
70-1074-PRS0089 In distribution
70-1207-IMP0012 In distribution
70-1207-IMP0007 In distribution
70-1073-PRA0108 In distribution
70-1073-PRA0109 In distribution
70-1073-PRA0125 In distribution
70-1073-PRA0127 In distribution
70-1074-PRS0077 In distribution
70-1207-IMP0002 In distribution
70-1207-IMP0018 In distribution
70-1073-PRA0107 In distribution
70-1073-PRA0120 In distribution
70-1074-PRS0085 In distribution
70-1074-PRS0087 In distribution
70-1073-PRA0100 In distribution
70-1207-IMP0013 In distribution
70-1207-IMP0004 In distribution
70-1074-PRS0092 In distribution
70-1073-PRA0103 In distribution
70-1074-PRS0079 In distribution
70-1073-PRA0094 In distribution
70-1073-PRA0104 In distribution
70-1073-PRA0119 In distribution
70-1073-PRA0128 In distribution
70-1207-IMP0009 In distribution
70-1073-PRA0126 In distribution
70-1073-PRA0111 In distribution
70-1074-PRS0086 In distribution
70-1073-PRA0099 In distribution
70-1073-PRA0123 In distribution
70-1073-PRA0093 In distribution
70-1074-PRS0078 In distribution
70-1074-PRS0080 In distribution
70-1207-IMP0017 In distribution
70-1072-PRC0087 In distribution
70-1074-PRS0090 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252582 2025-11-18
K240240 2024-07-12
K231940 2024-05-15
K231097 2023-11-14
K223496 2023-09-26
K191222 2019-08-05
K170044 2017-06-06
K160979 2016-11-04
K151798 2015-11-16
K151375 2015-10-07
K143515 2015-10-01
K141923 2015-01-06
K142118 2014-11-25
K142115 2014-11-13
K141211 2014-10-22
K121391 2012-12-10
K120858 2012-12-06
K121688 2012-10-12
K100993 2010-12-28

Recalls

1 of these is 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
2025-09-30 Class II Employee error Incorrect titanium screw, packaged with dental implant. 208 units

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