Instrument

Flexible Depth Gauge Remove AND Discard Plastic CAP Prior TO Autoclaving

Registry build 21.09.26
10manufacturers in China registered for this device type
94catalogue numbers in this listing
3510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (4), Shanghai (3), Zhejiang (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWL
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for Instrument
Listed by Howmedica Osteonics Corp, United States
FDA product code KWL
Device type Prosthesis, Hip, Hemi-, Femoral, Metal
Device class Class 2
Regulation 21 CFR 888.3360
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
510(k) K211703
Record published 2016-09-24
Record revised 2023-10-04 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Packaging Pack of 25
Sizes Lumen/inner diameter 22 to 44 mm; outer diameter 40 to 71 mm; length 3 to 30 mm; depth 80 mm
Distribution end date 2023-10-02
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Instrument
Catalogue number Size Status
2210-22E Alpha Code: E In distribution
2230-22F Alpha Code: F In distribution
I-H21103600 Diameter: 36.0 Millimeter In distribution
2200-22H Degree: 0.0 Degree In distribution
2200-40G Lumen/Inner Diameter 40.0 mm In distribution
0930-5-000 In distribution
2200-26F Degree: 0.0 Degree In distribution
1150-2352 Outer Diameter 52.0 mm In distribution
0580-30 Offset: 30.0 Millimeter In distribution
2200-44I Degree: 0.0 Degree In distribution
2111-3028 Diameter: 28.0 Millimeter In distribution
1440-1000 In distribution
2208-4048 Diameter: 48.0 Millimeter In distribution
8000-7703 Size: 3 In distribution
4845-7-967 Side: LEFT In distribution
6264-8-332R Taper Connection: V40? In distribution
2107-3325 Diameter: 3.3 Millimeter In distribution
I-H21103240 Diameter: 32.0 Millimeter In distribution
6264-8-628R Head Diameter: 28.0 Millimeter In distribution
1100-2210R Taper Connection: C-TPR In distribution
2208-6053R Side: RIGHT In distribution
6088-9-810 Depth 80.0 mm In distribution
2210-22I Lumen/Inner Diameter 22.0 mm In distribution
1235-0-601 Side: RIGHT In distribution
1020-5205 Size: 5 In distribution
0939-1-118M Thickness: 18.0 Millimeter In distribution
I-H1236HA00 Length 3.0 mm In distribution
0580-4450-4 Size: 4 In distribution
2270-22E Degree: 0.0 Degree In distribution
2240-28C Alpha Code: C In distribution
6264-3-236R Offset: 4.0 Millimeter In distribution
2200-44J Alpha Code: J In distribution
I-H1862HB11 Size: 11 In distribution
1118-6000 In distribution
2200-26E Degree: 0.0 Degree In distribution
1235-0-542 Side: LEFT In distribution
1100-2875R Offset: 7.5 Millimeter In distribution
1601-1700 In distribution
2208-4054 Diameter: 54.0 Millimeter In distribution
6842-6-365 Taper Connection: C-TPR In distribution
2200-26C Degree: 0.0 Degree In distribution
2240-28I Degree: 0.0 Degree In distribution
1110-1113 In distribution
5097-5820 Thickness: 20.0 Millimeter In distribution
1030-2240 Lumen/Inner Diameter 22.0 mm In distribution
2208-4063 Diameter: 63.0 Millimeter In distribution
6059-9-505 In distribution
1030-2648 Outer Diameter 48.0 mm In distribution
2240-22C Degree: 0.0 Degree In distribution
2208-4071 Diameter: 71.0 Millimeter In distribution
1100-1325 Diameter: 25.0 Millimeter In distribution
0581-1-504 Offset: 50.0 Millimeter In distribution
0932-3-000 In distribution
2200-36G Alpha Code: G In distribution
5097-6625 Outer Diameter 66.0 mm In distribution
2208-2060A Diameter: 60.0 Millimeter In distribution
2200-40E Lumen/Inner Diameter 40.0 mm In distribution
6825-9-953 Outer Diameter 53.0 mm In distribution
2200-22E Degree: 0.0 Degree In distribution
2208-2062A Diameter: 62.0 Millimeter In distribution
2208-4075 Diameter: 75.0 Millimeter In distribution
2240-22I Degree: 0.0 Degree In distribution
0580-4450-1 Offset: 50.0 Millimeter In distribution
1111-1003 Diameter: 21.5 Millimeter In distribution
2210-28J Lumen/Inner Diameter 28.0 mm In distribution
2250-32E Degree: 10.0 Degree In distribution
4845-2-965 Size: 5 In distribution
I-H21103212 Diameter: 32.0 Millimeter In distribution
2107-1014 In distribution
2240-22J Degree: 0.0 Degree In distribution
2124-1200 In distribution
4845-7-530 Taper Connection: V40? In distribution
2102-0439 Diameter: 39.0 Millimeter In distribution
I-H2108PR58 Diameter: 58.0 Millimeter In distribution
2208-6061L Outer Diameter 61.0 mm In distribution
1601-30132 Diameter: 30.0 Millimeter In distribution
2208-4070 Diameter: 70.0 Millimeter In distribution
1020-2737 Diameter: 37.0 Millimeter In distribution
2240-36E Degree: 0.0 Degree In distribution
6090-4-330 In distribution
2208-6071R Outer Diameter 71.0 mm In distribution
1212-0019 Length 19.0 mm In distribution
I-H2154RG78 In distribution
2107-0011 In distribution
I-H1605HA50 Diameter: 50.0 Millimeter Withdrawn
I-H1961H367 Taper Connection: V40? Withdrawn
I-H1961H363 Offset: 5.0 Millimeter Withdrawn
I-H1268TH10 Diameter: 36.0 Millimeter Withdrawn
I-H16193330 Length 30.0 mm Withdrawn
I-H0659HA69 Diameter: 69.0 Millimeter Withdrawn
I-H0659HA63 Diameter: 63.0 Millimeter Withdrawn
I-H0659HA47 Diameter: 47.0 Millimeter Withdrawn
I-H1718HF00 Withdrawn
I-H1961H366 Offset: 7.5 Millimeter Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ustar II Knee System United Orthopedic Corp. 115
Consensus Hip System Shalby Advanced Technologies, Inc. 95
Consensus® Hip System Consensus Orthopedics, Inc. 95
UHR Howmedica Osteonics Corp 75
Austin Moore Howmedica Osteonics Corp 67
B-P Total HIP System Endotec, Inc. 66
CS2 Acetabular Cup System Consensus Orthopedics, Inc. 64
DJO Surgical Encore Medical, L.P. 62
Restoration Howmedica Osteonics Corp 56
Optimom Modular Heads Corin Limited 49
Corin Unipolar Modular Head Corin Limited 36
Perfecta Microport Orthopedics Inc. 35

Showing 12 of 167. All products under Prosthesis, Hip, Hemi-, Femoral, Metal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K071471 2007-09-10
K014226 2002-01-25
K992570 1999-09-01

Recalls

3 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
2026-07-30 Not classified Process change control Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to 12,156 US
2024-06-19 Class II Employee error Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component
potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
18 units
2024-06-19 Class II Employee error Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component
potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
18 units
2024-06-19 Class II Employee error Mislabeled: the size on the package label of the UNITRAX Endoprosthesis Head Component
potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
12 units
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 24 2010-07-27
2009-01-06 Not classified Process control Product deviation : Specific lots of sprayed HA hip stems did not meet Stryker’s Internal Material Specification for tensile bond strength and crystallinity. 1,628 total stems, all varieties. 2012-06-25
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27
2007-10-26 Not classified Process control Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head. 360 total 2010-01-27

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