HyperFlex® Bunion Correction System

"Pack:Implant:Stainless Steel:1st Met plate - Sterile Pack- Small - Right"

Registry build 21.09.26
22manufacturers in China registered for this device type
35catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
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
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for HyperFlex® Bunion Correction System
Listed by HyperFlex Medical Inc, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Manufacturer
510(k) K241995
Record published 2025-06-12
Record revised 2025-11-20 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for HyperFlex® Bunion Correction System
Catalogue number Size Status
FB-2910-RT In distribution
HF-2121-LFT Small-Medium-Left In distribution
HF-2231-LFT In distribution
HF-2111-RT Small-Small-Right In distribution
HF-2231-RT Medium-Large-Right In distribution
HF-2311-RT Large-Small-Right In distribution
HF-2211-RT Medium-Small-Right In distribution
HF-2211-LFT Medium-Small-Left In distribution
HF-2221-RT Medium-Medium-Right In distribution
HF-2221-LFT Medium-Medium-Left In distribution
FB-2990 In distribution
FB-2010-LFT Small In distribution
FB-2020-RT Large In distribution
FB-2030-RT Large In distribution
HF-2331-RT Large-Large-Right In distribution
FB-2300-RT Large In distribution
FB-2300-LFT Large In distribution
HF-2321-RT Large-Medium-Right In distribution
FB-2020-LFT Medium In distribution
HF-2131-RT Small-Large-Right In distribution
HF-2121-RT Small-Medium-Right In distribution
FB-2100-LFT Small In distribution
HF-2131-LFT Small-Large-Left In distribution
FB-2200-LFT Medium In distribution
HF-2331-LFT Large-Large-Left In distribution
HF-2910-RT In distribution
HF-2111-LFT Small-Small-Left In distribution
FB-2030-LFT Large In distribution
HF-2311-LFT Large-Small-Left In distribution
FB-2910-LFT In distribution
FB-2100-RT Small In distribution
HF-2910-LFT In distribution
FB-2200-RT Medium In distribution
FB-2010-RT Small In distribution
HF-2321-LFT Large-Medium-Left In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252997 2025-12-11

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