Advance

ADVANCE® CRUCIFORM Size 3-4 KEELED MODULAR STEM HA COATED

Registry build 21.09.26
12manufacturers in China registered for this device type
107catalogue numbers in this listing
8510(k) clearances naming this product code
12recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MBH
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
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
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
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 Advance
Listed by Microport Orthopedics Inc., United States
FDA product code MBH
Device type Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3565
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-23
Record revised 2020-04-20 (version 4)

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 10 to 17 mm; outer diameter 15 to 38 mm

Catalogue Numbers

Catalogue numbers for Advance
Catalogue number Size Status
KTSLFM41 In distribution
KIMA512L Height 12 mm In distribution
KTSLFM60 In distribution
KSPM1556 Outer Diameter 15 mm In distribution
KTSLFM10 In distribution
KIMA210L Height 10 mm In distribution
KTTIHA21 In distribution
KTTIHA30 In distribution
KTSLFM50 In distribution
KTSCFM11 In distribution
KPON35MB Outer Diameter 35 mm In distribution
KSPP1556 Outer Diameter 15 mm In distribution
KTSCFM20 In distribution
KTSSFM31 In distribution
KFTCPN3R In distribution
KTTIHA10 In distribution
KTSCFM21 In distribution
KTSSFM41 In distribution
KTSLFM40 In distribution
KPON29SP Outer Diameter 29 mm In distribution
KIMA212L Height 12 mm In distribution
KSPM1512 Outer Diameter 15 mm In distribution
KTSCFM31 In distribution
KIMA217L Height 17 mm In distribution
KIMA312L Height 12 mm In distribution
KIMA214L Height 14 mm In distribution
KFTCPC1R In distribution
KTSCFM40 In distribution
KIMA112L Height 12 mm In distribution
KTSCFM60 In distribution
KIMA310L Height 10 mm In distribution
KTTIPC41 In distribution
KTSCFM50 In distribution
KTSLFM11 In distribution
KTSSFM20 In distribution
SPKT0043 In distribution
KFSCPC4R In distribution
KFTCPC4R In distribution
KTTIPC51 In distribution
KPON38ST Outer Diameter 38 mm In distribution
KTSSFM51 In distribution
KTTIHA41 In distribution
KFSCPC2R In distribution
KTSCFM41 In distribution
KTTIHA51 In distribution
KTSLFM31 In distribution
KFTCPC2R In distribution
KFSCPC1R In distribution
KIMA417L Height 17 mm In distribution
KFTCNN2R In distribution
KTSSFM30 In distribution
KIMA117L Height 17 mm In distribution
KTSCFM30 In distribution
KPON29MB Outer Diameter 29 mm In distribution
KSPP1534 Outer Diameter 15 mm In distribution
KIMA114L Height 14 mm In distribution
KFSCPC3R In distribution
KFTCNN3R In distribution
KTTIHA50 In distribution
KFSCPC5R In distribution
KIMA510L Height 10 mm In distribution
KTTIHA60 In distribution
KTSLFM21 In distribution
KFSCPC5L In distribution
KTSSFM10 In distribution
KPONTP26 Outer Diameter 26 mm In distribution
KIMA410L Height 10 mm In distribution
KSPM1534 Outer Diameter 15 mm In distribution
KTTIPC21 In distribution
KSPP1512 Outer Diameter 15 mm In distribution
KFTCNN4R In distribution
KFSCPC4L In distribution
KTSLFM30 In distribution
KFTCPC3R In distribution
KIMA110L Height 10 mm In distribution
KIMA517L Height 17 mm In distribution
KTSSFM40 In distribution
KFSCPC1L In distribution
KTTIHA20 In distribution
KTTIPC31 In distribution
KIMA317L Height 17 mm In distribution
KIMA514L Height 14 mm In distribution
KFTCPC6R In distribution
KTSCFM10 In distribution
SPKT0042 In distribution
KFTCPC5R In distribution
KTTIHA40 In distribution
KTSLFM51 In distribution
KFTCPN2R In distribution
KTTIHA11 In distribution
KPON32ST Outer Diameter 32 mm In distribution
KTSCFM51 In distribution
KTSSFM11 In distribution
SPKT0044 In distribution
KFTCPN4R In distribution
KTSSFM21 In distribution
KIMA314L Height 14 mm In distribution
KTTIPC25 In distribution
KFSCPC3L In distribution
KIMA414L Height 14 mm In distribution
KIMA410R Height 10 mm In distribution
KTTIHA31 In distribution
KTSSFM50 In distribution
KTSLFM20 In distribution
KTTIPC11 In distribution
KFSCPC2L In distribution
KTSCFM25 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy Microport Orthopedics Inc. 4,272
Triathlon Howmedica Osteonics Corp 712
Instrument Howmedica Osteonics Corp 709
Persona® Vivacit-E® Zimmer, Inc. 499
Arthrex® Arthrex, Inc. 494
Persona® Zimmer, Inc. 441
Legion Smith & Nephew, Inc. 397
U2 Total Knee System United Orthopedic Corp. 286
Attune Depuy (Ireland) 234
DJO Surgical Encore Medical, L.P. 191
Vanguard XP Instrumentation Biomet Orthopedics 150
Truliant® Exactech, Inc. 142

Showing 12 of 948. All products under Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253728 2026-08-21
K233507 2024-01-18
K213817 2022-01-05
K180317 2018-05-04
K170288 2017-06-15
K152298 2015-11-16
K143366 2015-01-21
K140735 2014-08-29

Recalls

11 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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
2024-10-29 Class II Labeling Change Control Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging. 32
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 98 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 47 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 86 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 110 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 34 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 38 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 134 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 77 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 36 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 169 units 2017-07-26
2016-06-21 Class I Use error ADVANCE(R) HA Coated tibial bases are being recalled due to a higher than expected revision rate as a result of component loosening. 60 units 2017-07-26

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