Vanguard 360 Revision System

43 catalogue numbers from 185403, listed by Biomet Orthopedics, United States, under Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
43catalogue numbers in this listing

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Zhejiang (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MBV
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
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

Record

Regulatory record for Vanguard 360 Revision System
Listed by Biomet Orthopedics, United States
FDA product code MBV
Device type Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3560
510(k) K093293
Record published 2015-10-24
Record revised 2025-05-30 (version 5)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Vanguard 360 Revision System
Catalogue number Size Status
185403 10 MM 62.5 MM In distribution
185407 10 MM 72.5 MM In distribution
185460 15 MM 55 MM In distribution
185390 10 MM 80 MM In distribution
185384 10 MM 65 MM In distribution
185342 5 MM 60 MM In distribution
185428 10 MM 75 MM In distribution
185410 10 MM 80 MM In distribution
185420 10 MM 55 MM In distribution
185404 10 MM 65 MM In distribution
185310 5 MM 80 MM In distribution
185325 5 MM 67.5 MM In distribution
185330 5 MM 80 MM In distribution
185327 5 MM 72.5 MM In distribution
185381 10 MM 57.5 MM In distribution
185383 10 MM 62.5 MM In distribution
185464 15 MM 65 MM In distribution
185405 10 MM 67.5 MM In distribution
185305 5 MM 67.5 MM In distribution
185486 15 MM 70 MM In distribution
185345 5 MM 67.5 MM In distribution
185483 15 MM 62.5 MM In distribution
185347 5 MM 72.5 MM In distribution
185304 5 MM 65 MM In distribution
185343 5 MM 62.5 MM In distribution
185468 15 MM 75 MM In distribution
185326 5 MM 70 MM In distribution
185466 15 MM 70 MM In distribution
185344 5 MM 65 MM In distribution
185480 15 MM 55 MM In distribution
185302 5 MM 60 MM In distribution
185340 5 MM 55 MM In distribution
185408 10 MM 75 MM In distribution
185425 10 MM 67.5 MM In distribution
185350 5 MM 80 MM In distribution
185488 15 MM 75 MM In distribution
185401 10 MM 57.5 MM In distribution
185320 5 MM 55 MM In distribution
185388 10 MM 75 MM In distribution
185346 5 MM 70 MM In distribution
185462 15 MM 60 MM In distribution
185322 5 MM 60 MM In distribution
185386 10 MM 70 MM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vanguard XP® Instrumentation Biomet Orthopedics 130
Vanguard Complete Knee System Biomet Orthopedics 106
Vanguard® 360 Instrument Biomet Orthopedics 98
Biomet® Knee System Biomet Orthopedics 94
Maxim Knee System Biomet Orthopedics 73
Vanguard Knee System Biomet Orthopedics 49
Vanguard Instrument Biomet Orthopedics 44
Biomet® 360 Biomet Orthopedics 39
Biomet® 360 Instrument Biomet Orthopedics 36
Vanguard 360 Biomet Orthopedics 30
Biomet 360 Knee System Biomet Orthopedics 27
Vanguard® SSK 360 Knee System Biomet Orthopedics 19

Showing 12 of 41. All products under Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

Recalls Naming This Product

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

Recalls naming the identifiers of Vanguard 360 Revision System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2020-12-01 Class II Process control Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure 21 units 2022-07-08
Biomet, Inc. 510(k) number 2018-08-02 Class II Under Investigation by firm The implant only has one bolt in the sterile package but it should have had two. 16 2019-04-25
Biomet, Inc. 510(k) number 2018-08-02 Class II Under Investigation by firm The implant only has one bolt in the sterile package but it should have had two. 16 2019-04-25
Biomet, Inc. 510(k) number 2016-08-08 Class II Process control The drill bit used to drill the hex pre-drilled hole in the screw head of the Tibial Augment Bolts included in the Vanguard 360 Revision Knee System was larger than allowable per the process specification. As a result, the hex geometry can 454 2017-06-05
Biomet, Inc. 510(k) number 2014-07-01 Class II Process change control The Vanguard 360 Femoral Boss Reamers were manufactured oversized to the print. The instrument may not fit into the mating component. 461 2015-10-30

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