A.L.P.S.T15 Multi-Directional Locking Screw

62 catalogue numbers from 110017934, listed by Biomet Orthopedics, United States, under Plate, Fixation, Bone. 22 manufacturers in China are registered for this product code.

Registry build 21.09.26
22manufacturers in China registered for this device type
62catalogue numbers in this listing
4510(k) clearances naming this product 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 A.L.P.S.T15 Multi-Directional Locking Screw
Listed by Biomet Orthopedics, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
510(k) K083843
Record published 2016-03-23
Record revised 2025-05-30 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for A.L.P.S.T15 Multi-Directional Locking Screw
Catalogue number Size Status
110017934 3.5MM X 34MM In distribution
110018042 3.5MM X 42MM In distribution
110018050 3.5MM X 50MM In distribution
110018022 3.5MM X 22MM In distribution
110017938 3.5MM X 38MM In distribution
110017999 3.5MM X 100MM In distribution
110018012 3.5MM X 12MM In distribution
110018054 3.5MM X 54MM In distribution
110018060 3.5MM X 60MM In distribution
110017944 3.5MM X 44MM In distribution
110017954 3.5MM X 54MM In distribution
110017948 3.5MM X 48MM In distribution
110018058 3.5MM X 58MM In distribution
110018016 3.5MM X 16MM In distribution
110017956 3.5MM X 56MM In distribution
110017960 3.5MM X 60MM In distribution
110018070 3.5MM X 70MM In distribution
110017920 3.5MM X 20MM In distribution
110017930 3.5MM X 30MM In distribution
110017940 3.5MM X 40MM In distribution
110017922 3.5MM X 22MM In distribution
110017918 3.5MM X 18MM In distribution
110017924 3.5MM X 24MM In distribution
110017952 3.5MM X 52MM In distribution
110018026 3.5MM X 26MM In distribution
110017916 3.5MM X 16MM In distribution
110017932 3.5MM X 32MM In distribution
110018030 3.5MM X 30MM In distribution
110018090 3.5MM X 90MM In distribution
110018048 3.5MM X 48MM In distribution
110017912 3.5MM X 12MM In distribution
110017910 3.5MM X 10MM In distribution
110018024 3.5MM X 24MM In distribution
110017946 3.5MM X 46MM In distribution
110017936 3.5MM X 36MM In distribution
110017975 3.5MM X 75MM In distribution
110018034 3.5MM X 34MM In distribution
110017958 3.5MM X 58MM In distribution
110017926 3.5MM X 26MM In distribution
110017914 3.5MM X 14MM In distribution
110018032 3.5MM X 32MM In distribution
110018055 3.5MM X 55MM In distribution
110018056 3.5MM X 56MM In distribution
110018036 3.5MM X 36MM In distribution
110018052 3.5MM X 52MM In distribution
110018065 3.5MM X 65MM In distribution
110017985 3.5MM X 85MM In distribution
110018044 3.5MM X 44MM In distribution
110018040 3.5MM X 40MM In distribution
110017965 3.5MM X 65MM In distribution
110017942 3.5MM X 42MM In distribution
110018080 3.5MM X 80MM In distribution
110018020 3.5MM X 20MM In distribution
110018046 3.5MM X 46MM In distribution
110018018 3.5MM X 18MM In distribution
110018038 3.5MM X 38MM In distribution
110018014 3.5MM X 14MM In distribution
110017950 3.5MM X 50MM In distribution
110017970 3.5MM X 70MM In distribution
110018010 3.5MM X 10MM In distribution
110017928 3.5MM X 28MM In distribution
110018028 3.5MM X 28MM 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
K243761 2025-02-19
K022515 2002-09-17
K020221 2002-04-02
K013657 2001-12-03

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of A.L.P.S.T15 Multi-Directional Locking Screw
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2020-12-23 Class II Device Design The instruments may become cold welded together when the drill is inserted through the Soft Tissue Guide. This prevents disassociation of the instruments and potentially leads to an increased chance of fracture of the drill. 174 systems 2023-04-13
Biomet, Inc. 510(k) number 2020-05-14 Class II Device Design Distributed to the field without having completed design history files or design transfer activities 15 OUS 2021-04-08
Biomet, Inc. 510(k) number 2020-05-14 Class II Device Design Distributed to the field without having completed design history files or design transfer activities 15 OUS 2021-04-08

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