Forte

32 catalogue numbers from 2480-10-40, listed by Zimmer, Inc., United States, under Screw, Fixation, Bone. 31 manufacturers in China are registered for this product code.

Registry build 21.09.26
31manufacturers in China registered for this device type
32catalogue numbers in this listing
12510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWC
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11

Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone

Record

Regulatory record for Forte
Listed by Zimmer, Inc., United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K142836
Record published 2015-10-16
Record revised 2024-02-19 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Length 10 to 40 mm

Catalogue Numbers

Catalogue numbers for Forte
Catalogue number Size Status
2480-10-40 4.0 mm Diameter In distribution
2480-10-41 Length 10 mm In distribution
2480-16-41 4.0 mm Diameter In distribution
2480-20-40 4.0 mm Diameter In distribution
2480-12-40 4.0 mm Diameter In distribution
2480-22-40 4.0 mm Diameter In distribution
2480-18-40 4.0 mm Diameter In distribution
2480-20-41 Length 20 mm In distribution
2480-16-40 4.0 mm Diameter In distribution
2480-14-41 Length 14 mm In distribution
2480-36-40 4.0 mm Diameter In distribution
2480-38-40 Length 38 mm In distribution
2480-26-40 4.0 mm Diameter In distribution
2480-32-40 Length 32 mm In distribution
2480-30-41 4.0 mm Diameter In distribution
2480-40-40 Length 40 mm In distribution
2480-34-41 4.0 mm Diameter In distribution
2480-22-41 4.0 mm Diameter In distribution
2480-28-40 Length 28 mm In distribution
2480-24-41 4.0 mm Diameter In distribution
2480-38-41 Length 38 mm In distribution
2480-12-41 4.0 mm Diameter In distribution
2480-34-40 4.0 mm Diameter In distribution
2480-28-41 4.0 mm Diameter In distribution
2480-18-41 4.0 mm Diameter In distribution
2480-24-40 Length 24 mm In distribution
2480-14-40 Length 14 mm In distribution
2480-32-41 4.0 mm Diameter In distribution
2480-30-40 Length 30 mm In distribution
2480-40-41 4.0 mm Diameter In distribution
2480-36-41 Length 36 mm In distribution
2480-26-41 Length 26 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Screw, Fixation, Bone Synthes Gmbh 3,975
Aptus Medartis Inc. 3,623
Acumed Acumed LLC 3,187
Arthrex® Arthrex, Inc. 2,781
OsteoMed Osteomed 2,764
Screw, Fixation, Bone AAP Implantate AG 2,176
Screw, Fixation, Bone Zimmer, Inc. 1,993
Arix System Bone Screw Jeil Medical Corporation 1,875
Cannulated Screw System + Tyber Medical 1,814
Cannulated Compression Headless Screw Tyber Medical 1,621
Microware Bone Plates and Bone Screws Microware Precision Co., Ltd. 1,601
Anthem Globus Medical, Inc. 1,538

Showing 12 of 5,775. All products under Screw, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K152841 2015-11-24
K143165 2015-03-31
K142442 2014-10-03
K130810 2013-09-19
K112885 2011-12-19
K111447 2011-10-05
K101696 2010-09-10
K070906 2007-05-01
K060710 2006-04-26
K051098 2005-07-07
K946347 1995-07-11
K792022 1979-10-26

Recalls

40 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
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2024-03-20 Class II Under Investigation by firm Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in s
2019-10-10 Class II Packaging change control Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration). 5,459,583 total devices 2020-05-19
2015-12-09 Class II Labeling Change Control Product on the package label did not match what was inside the package.
The label was for part number 00-2359-058-35 (Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58mm Length) lot number 62918019 while the product inside
400 2016-11-08
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. Specifically, multiple test samples from
each of the six configurations faile
972,125 units 2015-09-15
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2014-07-22 Class II Package design/selection Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only. 47,682 units total 2015-06-18
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14
2013-10-11 Class II Packaging Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 7,044,680 total 2017-04-14

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