Inbone™ Everlast™

48 catalogue numbers from 22022116, listed by Wright Medical Technology, Inc., United States, under Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
48catalogue numbers in this listing
9recalls on this code

Who Else Makes It

Registered in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HSN
Manufacturer City Province Registered as Device types
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10

Record

Regulatory record for Inbone™ Everlast™
Listed by Wright Medical Technology, Inc., United States
FDA product code HSN
Device type Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3110
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2020-07-07
Record revised 2022-06-17 (version 3)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Sizes Height 6 to 20 mm

Catalogue Numbers

Catalogue numbers for Inbone™ Everlast™
Catalogue number Size Status
22022116 Height 16 mm In distribution
22022214 Height 14 mm In distribution
22024417 Height 17 mm In distribution
22024320 Height 20 mm In distribution
22025414 Height 14 mm In distribution
22025420 Height 20 mm In distribution
22022210 Height 10 mm In distribution
22022110 Height 8 mm In distribution
22024419 Height 19 mm In distribution
22025412 Height 12 mm In distribution
22023210 Height 10 mm In distribution
22025509 Height 9 mm In distribution
22024314 Height 14 mm In distribution
22024409 Height 9 mm In distribution
22024415 Height 15 mm In distribution
22025511 Height 11 mm In distribution
22025418 Height 18 mm In distribution
22025513 Height 13 mm In distribution
22023316 Height 16 mm In distribution
22022212 Height 12 mm In distribution
22025515 Height 15 mm In distribution
22023314 Height 14 mm In distribution
22023214 Height 14 mm In distribution
22025517 Height 17 mm In distribution
22022208 Height 8 mm In distribution
22022114 Height 14 mm In distribution
22025416 Height 16 mm In distribution
22023218 Height 18 mm In distribution
22023308 Height 8 mm In distribution
22024316 Height 16 mm In distribution
22023216 Height 16 mm In distribution
22025519 Height 19 mm In distribution
22024318 Height 18 mm In distribution
22024413 Height 13 mm In distribution
22022108 Height 8 mm In distribution
22022106 Height 6 mm In distribution
22022206 Height 6 mm In distribution
22024411 Height 11 mm In distribution
22023312 Height 12 mm In distribution
22025410 Height 10 mm In distribution
22023208 Height 8 mm In distribution
22022216 Height 16 mm In distribution
22024312 Height 12 mm In distribution
22024310 Height 10 mm In distribution
22022112 Height 12 mm In distribution
22023310 Height 10 mm In distribution
22023318 Height 18 mm In distribution
22023212 Height 12 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Apex 3D Total Ankle Replacement System Paragon 28 658
Vantage Exactech, Inc. 362
Cadence™ Ascension Orthopedics, Inc. 248
Cadence Total Ankle System Smith & Nephew, Inc. 246
Inbone Wright Medical Technology, Inc. 236
Hintermann Series H2 DT Medtech LLC 225
Infinity Wright Medical Technology, Inc. 220
Incompass Total Ankle System Wright Medical Technology, Inc. 213
Invision Wright Medical Technology, Inc. 186
Kinos Axiom Instrumentation restor3d, inc. 169
Quantum In2Bones SAS 157
Hintermann Series H2 Vilex LLC 153

Showing 12 of 53. All products under Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Recalls

9 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
2024-03-06 Class II Process change control Stryker has identified an issue that impacts specific lots of Infinity” Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing 47 units
2023-06-13 Class II Process control The devices were manufactured with the pin sleeve holes too narrow, which does not allow the pin sleeves to pass through the pin sleeve holes, thereby preventing pin placement through the pin holes. 106 devices
2022-09-30 Class II Device Design The tibial tray lock detail is oversized (larger than specification). 1 unit 2026-08-21
2022-09-30 Class II Device Design The tibial tray lock detail is oversized (larger than specification). 1 unit 2026-08-21
2022-06-02 Class II Nonconforming Material/Component The instrument is incorrectly color coded. 35 units
2021-11-04 Class II Nonconforming Material/Component The package contents and package labeling do not match. 2 units 2023-01-06
2021-11-04 Class II Nonconforming Material/Component The package contents and package labeling do not match. 0 (2 Quarantined) 2023-01-06
2020-04-09 Class II Nonconforming Material/Component One lot of INBONE Tibial Trays is missing the plasma coating. 22 units 2020-11-02
2016-11-08 Class II Process control The firm discovered a lack of adequate documentation confirming sterility on certain products. 65 units 2020-11-03

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