FPS

5th Metatarsal Avulsion Fracture Hook Plate, 5 Hole, Right

Registry build 21.09.26
22manufacturers in China registered for this device type
119catalogue numbers in this listing
11510(k) clearances naming this product code
20recalls on this code

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 FPS
Listed by Tyber Medical, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2022-12-15
Record revised 2025-11-20 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for FPS
Catalogue number Size Status
M25-733001 In distribution
M25-501030 In distribution
M25-713040 In distribution
M25-713050 In distribution
M25-602050 In distribution
M25-728011 In distribution
M25-605032 In distribution
M25-714042 In distribution
M25-711151 In distribution
M25-711251 In distribution
M25-501050 In distribution
M25-610000 In distribution
M25-711102 In distribution
M25-605042 In distribution
M25-605052 In distribution
M25-734001 In distribution
M25-702040 In distribution
M25-604040 In distribution
M25-712251 In distribution
M25-503040 In distribution
M25-502030 In distribution
M25-727021 In distribution
M25-614003 In distribution
M25-603060 In distribution
M25-602030 In distribution
M25-714041 In distribution
M25-732032 In distribution
M25-713060 In distribution
M25-614002 In distribution
M25-705020 In distribution
M25-616002 In distribution
M25-603040 In distribution
M25-608011 In distribution
M25-721051 In distribution
M25-615002 In distribution
M25-732031 In distribution
M25-601040 In distribution
M25-728032 In distribution
M25-618002 In distribution
M25-702020 In distribution
M25-728012 In distribution
M25-503050 In distribution
M25-608012 In distribution
M25-702030 In distribution
M25-608031 In distribution
M25-711201 In distribution
M25-727031 In distribution
M25-601070 In distribution
M25-503060 In distribution
M25-609030 In distribution
M25-734011 In distribution
M25-605051 In distribution
M25-727022 In distribution
M25-604030 In distribution
M25-713030 In distribution
M25-605031 In distribution
M25-603050 In distribution
M25-727012 In distribution
M25-607000 In distribution
M25-728021 In distribution
M25-605061 In distribution
M25-604060 In distribution
M25-711202 In distribution
M25-733011 In distribution
M25-615001 In distribution
M25-712252 In distribution
M25-502050 In distribution
M25-734021 In distribution
M25-601060 In distribution
M25-605062 In distribution
M25-614001 In distribution
M25-601030 In distribution
M25-616001 In distribution
M25-601050 In distribution
M25-603030 In distribution
M25-721032 In distribution
M25-714021 In distribution
M25-721041 In distribution
M25-721052 In distribution
M25-602040 In distribution
M25-721031 In distribution
M25-711152 In distribution
M25-706030 In distribution
M25-722030 In distribution
M25-503030 In distribution
M25-732012 In distribution
M25-617002 In distribution
M25-711101 In distribution
M25-714022 In distribution
M25-618001 In distribution
M25-722040 In distribution
M25-702050 In distribution
M25-702060 In distribution
M25-733012 In distribution
M25-727011 In distribution
M25-609010 In distribution
M25-728031 In distribution
M25-604050 In distribution
M25-722050 In distribution
M25-732011 In distribution
M25-501040 In distribution
M25-502040 In distribution
M25-608032 In distribution
M25-602060 In distribution
M25-706010 In distribution
M25-705030 In distribution
M25-711252 In distribution
M25-714001 In distribution
M25-721042 In distribution
M25-617001 In distribution
M25-733002 In distribution
M25-714002 In distribution
M25-705010 In distribution
M25-501060 In distribution
M25-502060 In distribution
M25-727032 In distribution
M25-605041 In distribution
M25-706020 In distribution
M25-728022 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
K261207 2026-06-12
K251361 2025-07-30
K242486 2025-03-19
K241218 2024-05-31
K233423 2023-12-21
K233017 2023-12-20
K232652 2023-12-13
K232693 2023-12-04
K222465 2023-03-07
K203817 2021-08-13
K193222 2020-01-20

Recalls

20 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
2025-12-19 Class II Process control The supplier manufactured anatomical left plates with an incorrect thread orientation. 100 units
2025-12-19 Class II Process control The supplier manufactured anatomical left plates with an incorrect thread orientation. 64 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 408
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 200 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 212 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 412 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 201 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 109 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 418 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 100 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 219 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 214 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 208 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 397
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 197 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 100 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 115 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 209 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 220 units
2025-01-21 Class II Process control Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices 210 units

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