Soft Face Mallet

Soft Face Mallet 750 gram

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Shanghai (2), Shandong (1).

Chinese manufacturers registered for FDA product code GFJ
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Shanghai Kangqiao Dental Instruments Factory Shanghai Shanghai Manufacturer 54

Record

Regulatory record for Soft Face Mallet
Listed by Signal Medical Corp., United States
FDA product code GFJ
Device type Mallet, Surgical, General & Plastic Surgery
Device class Class 1
Regulation 21 CFR 878.4800
Premarket notification Exempt
Record published 2021-10-15

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization

Catalogue Numbers

Catalogue numbers for Soft Face Mallet
Catalogue number Size Status
750 gram In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sklar® Sklar Corporation 86
Millennium Avalign Technologies, Inc. 67
gSource Gsource, LLC. 62
Boss Instruments Boss Instruments, Ltd. 43
Ambler Surgical Ambler Surgical, LLC 39
Surtex Surtex Instruments Ltd 36
Novo Surgical Inc. Novo Surgical, Inc. 30
Orthomed Ortho-MED, Inc. 28
HNM Medical HNM Stainless, LLC. 26
Kmedic Teleflex Medical LLC 23
Avalign Avalign Technologies, Inc. 23
V. Mueller Steris Corporation 22

Showing 12 of 91. All products under Mallet, Surgical, General & Plastic Surgery

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 Closed
2017-02-20 Class II Labeling design Potential for poly tip of the mallet to come off during use. Potential for foreign material in the surgical field or delay in surgery. Reminder for customers that the poly tip must be removed for cleaning and sterilization to assure proper 1,640 2017-08-25

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