PediNail

Headless Locking Bolt, 30MM

Registry build 21.09.26
17manufacturers in China registered for this device type
54catalogue numbers in this listing
6510(k) clearances naming this product code
31recalls on this code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (3). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HSB
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
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
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 17. All 17 manufacturers in China registered for Rod, Fixation, Intramedullary And Accessories

Record

Regulatory record for PediNail
Listed by Orthopediatrics, Corp, United States
FDA product code HSB
Device type Rod, Fixation, Intramedullary And Accessories
Device class Class 2
Regulation 21 CFR 888.3020
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K083726
Record published 2016-10-31
Record revised 2025-07-14 (version 5)

Specifications

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

Catalogue Numbers

Catalogue numbers for PediNail
Catalogue number Size Status
00-1500-5068 In distribution
00-1500-5098 In distribution
00-1500-5062 In distribution
00-1500-5056 In distribution
00-1500-5094 In distribution
00-1500-5050 In distribution
00-1500-5085 In distribution
00-1500-5044 In distribution
00-1500-5052 In distribution
00-1500-5022 In distribution
00-1500-5055 In distribution
00-1500-5075 In distribution
00-1500-5082 In distribution
00-1500-5036 In distribution
00-1500-5048 In distribution
00-1500-5096 In distribution
00-1500-6530 In distribution
00-1500-5046 In distribution
00-1500-5086 In distribution
00-1500-5080 In distribution
00-1500-5034 In distribution
00-1500-5035 In distribution
00-1500-5020 In distribution
00-1500-5095 In distribution
00-1500-5065 In distribution
00-1500-5064 In distribution
00-1500-5072 In distribution
00-1500-5088 In distribution
00-1500-5092 In distribution
00-1500-5084 In distribution
00-1500-5025 In distribution
00-1500-5042 In distribution
00-1500-5028 In distribution
00-1500-5054 In distribution
00-1500-6560 In distribution
00-1500-5066 In distribution
00-1500-6532 In distribution
00-1500-5070 In distribution
00-1500-5024 In distribution
00-1500-5078 In distribution
00-1500-5000 In distribution
00-1500-5040 In distribution
00-1500-5032 In distribution
00-1500-5038 In distribution
00-1500-5030 In distribution
00-1500-5026 In distribution
00-1500-5018 In distribution
00-1500-5076 In distribution
00-1500-5045 In distribution
00-1500-5060 In distribution
00-1500-5074 In distribution
00-1500-5016 In distribution
00-1500-5090 In distribution
00-1500-5058 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
T2 Stryker GmbH 1,373
Autobahn Globus Medical, Inc. 1,258
Gamma Stryker GmbH 1,120
Summa Orthopaedics Femur Nail System Jeil Medical Corporation 742
Arix Femur Nail System Jeil Medical Corporation 742
Orthofix Orthofix SRL 721
Rod, Fixation, Intramedullary And Accessories Synthes Gmbh 715
Trigen Smith & Nephew, Inc. 681
Arthrex® Arthrex, Inc. 665
Precice® Intramedullary Limb Lengthening System NuVasive Specialized Orthopedics, Inc. 596
Apex Orthoxel Designated Activity Company 569
Natural Nail® Zimmer, Inc. 552

Showing 12 of 2,207. All products under Rod, Fixation, Intramedullary And Accessories

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K250623 2025-04-01
K231266 2023-08-21
K220679 2022-07-20
K190321 2019-10-09
K172583 2018-05-10
K083726 2009-03-11

Recalls Naming This Product

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

Recalls naming the identifiers of PediNail
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Orthopediatrics, Corp 510(k) number 2016-11-18 Class III Labeling mix-ups Labeled as a 48mm Cortical Screw but measuring at 50mm 22 units 2017-07-27
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25
Orthopediatrics, Corp 510(k) number 2009-07-21 Not classified Device Design The potential exists for the nails to fracture during insertion of the nail. 23 of all products 2010-10-25

Recalls

4 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
2019-08-19 Class II Nonconforming Material/Component Binding can occur between the attachment bolt and intramedullary nail, which may lead to delays in surgical procedures. 969 total 2020-04-30
2019-08-19 Class II Nonconforming Material/Component Binding can occur between the attachment bolt and intramedullary nail, which may lead to delays in surgical procedures. 969 total 2020-04-30
2019-08-19 Class II Device Design Interference can occur between the adolescent attachment bolt and the adolescent nail, cause a delay in surgical procedures 211 units 2020-10-26
2012-09-13 Class II Reprocessing Controls A complaint received from sales representative that a replenishment instrument was too short. Upon investigation, it has been determined that the device was not manufactured to design specifications and will not function as intended. 78 2013-09-18

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