Omni Interface Acetabular System

ApeX-LNK Crosslinked Acetabular Insert, UHMWPE 10 degree Hood +4mm Offset, F Insert, 40mm ID

Registry build 21.09.26
14manufacturers in China registered for this device type
104catalogue numbers in this listing
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LPH
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
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Record

Regulatory record for Omni Interface Acetabular System
Listed by Omni Life Science, Inc., United States
FDA product code LPH
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Record published 2015-11-27
Record revised 2021-09-13 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Omni Interface Acetabular System
Catalogue number Size Status
H5-12370 In distribution
H6-15236 In distribution
H5-54128 In distribution
H5-12368 In distribution
H5-12064 In distribution
400000 In distribution
H6-05240 In distribution
H6-03928 In distribution
H5-11354 In distribution
H5-12060 In distribution
H5-12360 In distribution
H5-12062 In distribution
H5-12356 In distribution
H5-12058 In distribution
H4-04128 In distribution
434828 In distribution
H5-12350 In distribution
H5-12366 In distribution
H5-11054 In distribution
H5-12364 In distribution
H6-04840 In distribution
410360 In distribution
410362 In distribution
H4-05236 In distribution
410354 In distribution
410350 In distribution
H5-12046 In distribution
H6-14840 In distribution
H5-11350 In distribution
H5-11352 In distribution
434132 In distribution
H6-04436 In distribution
433728 In distribution
H6-04836 In distribution
H5-12048 In distribution
434128 In distribution
410048 In distribution
413928 In distribution
410064 In distribution
H5-11058 In distribution
H5-55228 In distribution
410370 In distribution
410346 In distribution
H5-44832 In distribution
H6-13728 In distribution
414432 In distribution
410066 In distribution
H4-04432 In distribution
H5-11356 In distribution
H5-12050 In distribution
H5-12354 In distribution
434832 In distribution
H5-11048 In distribution
H5-12352 In distribution
H5-12346 In distribution
H5-12348 In distribution
435228 In distribution
414428 In distribution
H5-11052 In distribution
H5-55236 In distribution
H5-44132 In distribution
410054 In distribution
H6-14836 In distribution
H4-03928 In distribution
410356 In distribution
410058 In distribution
H6-03728 In distribution
410368 In distribution
410364 In distribution
H6-13928 In distribution
H5-55232 In distribution
H5-12066 In distribution
H5-12362 In distribution
H5-12052 In distribution
H5-11056 In distribution
410352 In distribution
410348 In distribution
H5-11050 In distribution
H5-12056 In distribution
H5-12054 In distribution
H6-15240 In distribution
H5-12358 In distribution
410046 In distribution
414132 In distribution
413728 In distribution
H6-04132 In distribution
410056 In distribution
H5-44836 In distribution
H5-44432 In distribution
H5-54132 In distribution
410052 In distribution
410050 In distribution
410060 In distribution
H6-14436 In distribution
H5-11358 In distribution
H6-05236 In distribution
434428 In distribution
H5-54832 In distribution
410366 In distribution
415228 In distribution
410062 In distribution
H5-11348 In distribution
410358 In distribution
H6-14132 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Initia Total Hip System Kyocera Medical Technologies, Inc. 1,000
DJO Surgical Encore Medical, L.P. 624
Pinnacle Depuy Orthopaedics, Inc. 613
Trilogy® Longevity® Zimmer, Inc. 564
Instrument Howmedica Osteonics Corp 369
InSitu Hip System Nextstep Arthropedix 368
Trilogy® Zimmer, Inc. 359
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 298
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Zimmer, Inc. 286
Bencox Hip System Corentec Co., Ltd. 286
OrthoMedFlex Orthomedflex LLC 257
Sterizo Total Hip System CPM Medical Consultants, LLC. 240

Showing 12 of 792. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K113242 2012-01-05
K110947 2011-06-16
K101976 2010-09-14
K100555 2010-03-29
K092443 2009-10-23
K073150 2008-02-27
K060072 2006-08-24

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P880025 1991-12-04 AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS Depuy Intl., Ltd.
P880076 1991-06-17 WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS Dow Corning Wright
P850061 1991-03-08 BIAS(R) FIBER METAL TOTAL HIP SYSTEM Zimmer, Inc.

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