Aesculap

SC/MSC Trial Insert 32MM 56/58 Post.wall

Registry build 21.09.26
21manufacturers in China registered for this device type
143catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (3), Zhejiang (2). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWT
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Guangzhou Clean Medical Products Manufacturing Corp Guangzhou Guangdong Contract manufacturer 5
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Showing 12 of 21. All 21 manufacturers in China registered for Template

Record

Regulatory record for Aesculap
Listed by Aesculap AG, Germany
FDA product code HWT
Device type Template
Device class Class 1
Regulation 21 CFR 888.4800
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-04-23
Record revised 2025-11-13 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2025-01-22
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Aesculap
Catalogue number Size Status
NG966R In distribution
NG952R In distribution
NG506 In distribution
NG958R In distribution
NG964R In distribution
NG503 In distribution
NG944R In distribution
NG950R In distribution
NG948R In distribution
NG942R In distribution
NG954R In distribution
NG960R In distribution
NG968R In distribution
NG946R In distribution
NG962R In distribution
NG940R In distribution
NG956R In distribution
NG305 Withdrawn
ND925 Withdrawn
NF753 Withdrawn
NT1189 Withdrawn
ND929 Withdrawn
NG328 Withdrawn
ND912 Withdrawn
NF724 Withdrawn
NG505 Withdrawn
NG283 Withdrawn
ND915 Withdrawn
NQ285 Withdrawn
NT976 Withdrawn
ND924 Withdrawn
NG393 Withdrawn
NG496 Withdrawn
NG303 Withdrawn
NG309 Withdrawn
NG301 Withdrawn
NT980 Withdrawn
NF770R Withdrawn
NF755 Withdrawn
NF723 Withdrawn
NT958 Withdrawn
NT969 Withdrawn
NG342 Withdrawn
NF757 Withdrawn
NF756 Withdrawn
ND923 Withdrawn
NF726 Withdrawn
ND921 Withdrawn
NT959 Withdrawn
NG514 Withdrawn
ND931 Withdrawn
ND927 Withdrawn
ND926 Withdrawn
NG495 Withdrawn
NG645 Withdrawn
NQ286 Withdrawn
NG327 Withdrawn
NG326 Withdrawn
NE100T Withdrawn
NQ284 Withdrawn
NF750 Withdrawn
NT977 Withdrawn
ND917 Withdrawn
NF762 Withdrawn
NF752 Withdrawn
NF754 Withdrawn
NE090T Withdrawn
NT1116 Withdrawn
NF725 Withdrawn
NG319 Withdrawn
NG502 Withdrawn
NG345 Withdrawn
NT1190 Withdrawn
NG318 Withdrawn
NT1159R Withdrawn
ND922 Withdrawn
NF748 Withdrawn
ND918 Withdrawn
NT947 Withdrawn
ND913 Withdrawn
ND919 Withdrawn
NT1137R Withdrawn
NG302 Withdrawn
ND914 Withdrawn
NT1188 Withdrawn
NF749 Withdrawn
ND920 Withdrawn
NG299 Withdrawn
NT966 Withdrawn
NQ283 Withdrawn
NQ282 Withdrawn
NG344 Withdrawn
NF751 Withdrawn
NG281 Withdrawn
NF747 Withdrawn
NT957 Withdrawn
ND911 Withdrawn
NF759 Withdrawn
NG320 Withdrawn
NG304 Withdrawn
NT968 Withdrawn
NT978 Withdrawn
NG343 Withdrawn
NT1118 Withdrawn
NG282 Withdrawn
NF722 Withdrawn
NG310 Withdrawn
NT960 Withdrawn
NT1186 Withdrawn
NG642 Withdrawn
NF771R Withdrawn
NT967 Withdrawn
NT1156R Withdrawn
NT970 Withdrawn
NG316 Withdrawn
NG641 Withdrawn
NG317 Withdrawn
NF721 Withdrawn
ND916 Withdrawn
NG513 Withdrawn
NG341 Withdrawn
NG296 Withdrawn
NT1117 Withdrawn
ND928 Withdrawn
NF758 Withdrawn
NT1136R Withdrawn
NG297 Withdrawn
NT956 Withdrawn
NG643 Withdrawn
NG504 Withdrawn
NG394 Withdrawn
ND909 Withdrawn
NG646 Withdrawn
NG329 Withdrawn
NG307 Withdrawn
NT1187 Withdrawn
NG395 Withdrawn
NT1157R Withdrawn
NG300 Withdrawn
NT948 Withdrawn
NT1138R Withdrawn
NQ281 Withdrawn
NT979 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Attune Depuy (Ireland) 1,385
Template Exactech, Inc. 1,277
4WEB Medical 4WEB Inc. 991
Evolution® Microport Orthopedics Inc. 966
Template Zimmer, Inc. 792
Advance® Microport Orthopedics Inc. 644
Apex Knee System Omni Life Science, Inc. 635
Profemur® Microport Orthopedics Inc. 591
Link Instruments – Trial implants and size gauges Waldemar Link GmbH & Co. KG 549
Template Synthes Gmbh 516
Optetrak Logic Exactech, Inc. 512
Template Depuy Spine, Inc. 451

Showing 12 of 2,940. All products under Template

Recalls

2 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
2017-08-10 Class II Mixed-up of materials/components The NS357R Vega PS Tibia Trial/Preparation Plateau size T4 may be incorrectly labeled. If the incorrect size trial is used the potential risk is implantation of the incorrect implant size which may lead to injury of ligaments, pain and pos 13 Units 2018-08-08
2012-07-12 Class II Employee error The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are correctly dimensioned, but the part number etched on the instrument may be incorrect. The 4 degree trial instrument (SJ768T-US) may be marked with the incorrect part num 5 2013-02-22

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