Ender Nail

4.0MM Diameter Nail 4.00MMX28CM Formerly Ender

Registry build 21.09.26
3manufacturers in China registered for this device type
82catalogue numbers in this listing
12510(k) clearances naming this product code
8recalls on this code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code JDS
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Record

Regulatory record for Ender Nail
Listed by Smith & Nephew, Inc., United States
FDA product code JDS
Device type Nail, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K983942
Record published 2015-09-28
Record revised 2025-02-06 (version 6)

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
Distribution end date 2023-09-28

Catalogue Numbers

Catalogue numbers for Ender Nail
Catalogue number Size Status
224025 In distribution
224027 In distribution
224036 In distribution
223525 In distribution
223538 In distribution
223528 In distribution
224031 In distribution
224538 In distribution
224038 In distribution
224026 In distribution
223526 In distribution
224022 In distribution
223529 In distribution
224545 In distribution
224034 In distribution
224033 In distribution
224527 In distribution
224535 In distribution
224536 In distribution
224030 In distribution
223522 In distribution
223535 In distribution
224544 In distribution
224540 In distribution
224542 In distribution
224024 In distribution
224547 In distribution
224548 In distribution
223537 In distribution
223536 In distribution
223534 In distribution
224549 In distribution
223532 In distribution
223530 In distribution
224029 In distribution
223533 In distribution
224032 In distribution
224543 In distribution
224541 In distribution
224037 In distribution
224035 In distribution
223524 In distribution
224533 In distribution
224539 In distribution
224534 In distribution
223523 In distribution
224537 In distribution
223531 In distribution
224546 In distribution
224028 In distribution
223527 In distribution
224023 In distribution
224532 In distribution
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Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Autobahn Globus Medical, Inc. 1,102
Trigen Smith & Nephew, Inc. 1,062
Nail, Fixation, Bone Synthes Gmbh 296
Nail, Fixation, Bone Synthes (U.S.A.) LP 237
Intertan MAX Smith & Nephew, Inc. 235
EXPert Nail Synthes Gmbh 225
Trigen MAX Smith & Nephew, Inc. 172
Ajax Nail Auxein medical Private limited 168
GPC GPC Medical Limited 155
130° Ga-mma Nail Auxein medical Private limited 90
Centronail Titanium Humeral Nailing System Orthofix SRL 79
Expert Femoral Nail Auxein medical Private limited 70

Showing 12 of 112. All products under Nail, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243608 2025-06-12
K240061 2024-09-20
K241804 2024-08-22
K230761 2023-06-14
K123948 2013-03-14
K061783 2006-08-10
K061019 2006-06-06
K051557 2005-06-30
K050938 2005-05-04
K040212 2004-02-20
K983942 1998-12-04
K981529 1998-07-09

Recalls

8 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
2020-11-02 Class II Packaging process control Manufacturing packaging error. 41 units 2023-01-06
2020-06-24 Class II Reprocessing Controls A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve. 12 units 2021-04-28
2017-10-24 Class II Employee error A single lot of INTERTAN 10S 10 MM X 18 CM 130 D was manufactured with the screw inserted upside down. 17 units
2014-07-02 Class II Under Investigation by firm There was an error in manufacturing which resulted in the proximal lag screw hole being positioned incorrectly in several batches of TRIGEN(R); INTERTAN(TM); NAILS. 601 units 2019-08-20
2014-04-04 Class II Process control A manufacturing error resulted in the set screw being inserted too deep in the affected nails. 1,253 units total 2017-07-01
2014-04-04 Class II Process control A manufacturing error resulted in the set screw being inserted too deep in the affected nails. 1,253 units total 2017-07-01
2013-02-07 Class II Labeling mix-ups 75 mm screws were packaged and labeled using an 80 mm screw outer box and label, while 80 mm screws were packaged and labeled using a 75 mm screw outer box and label. 90 units 2016-01-11
2013-02-07 Class II Labeling mix-ups 75 mm screws were packaged and labeled using an 80 mm screw outer box and label, while 80 mm screws were packaged and labeled using a 75 mm screw outer box and label. 69 units 2016-01-11

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