Plasmafit

Plasmafit Tray F/Module Trial Cups

Registry build 21.09.26
21manufacturers in China registered for this device type
81catalogue 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 Plasmafit
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 2020-04-24
Record revised 2025-11-13 (version 5)

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 Plasmafit
Catalogue number Size Status
NT456R In distribution
NT614 In distribution
NT684 In distribution
NT707 In distribution
NT460R In distribution
NT464R In distribution
NT450R In distribution
NT482 In distribution
NT591 In distribution
NT452R In distribution
NT483 In distribution
NT615 In distribution
NT704 In distribution
NT448R In distribution
NT613 In distribution
NT491 In distribution
NT617 In distribution
NT484 In distribution
NT502 In distribution
NT440R In distribution
NT616 In distribution
NT589 In distribution
NT519 In distribution
NT508 In distribution
NT609 In distribution
NT682 In distribution
NT513 In distribution
NT458R In distribution
NT706 In distribution
NT527 In distribution
NT504 In distribution
NT709 In distribution
NT701 In distribution
NT605 In distribution
NT584 In distribution
NT454R In distribution
NT506 In distribution
NT514 In distribution
NT705 In distribution
NT708 In distribution
NT702 In distribution
NT608 In distribution
NT619 In distribution
NT466R In distribution
NT690 In distribution
NT501 In distribution
NT515 In distribution
NT526 In distribution
NT604 In distribution
NT603 In distribution
NT691 In distribution
NT582 In distribution
NT462R In distribution
NT442R In distribution
NT618 In distribution
NT601 In distribution
NT703 In distribution
NT689 In distribution
NT503 In distribution
NT602 In distribution
NT509 In distribution
NT444R In distribution
NT683 In distribution
NT470R In distribution
NT468R In distribution
NT489 In distribution
NT490 In distribution
NT505 In distribution
NT446R In distribution
NT529 In distribution
NT507 In distribution
NT607 In distribution
NT516 In distribution
NT528 In distribution
NT525 In distribution
NT517 In distribution
NT590 In distribution
NT606 In distribution
NT518 In distribution
NT437R In distribution
NT583 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