Omnifit

Universal Distal Cement Spacer

Registry build 21.09.26
13manufacturers in China registered for this device type
149catalogue numbers in this listing
17510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDI
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
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
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
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing 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
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Showing 12 of 13. All 13 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Record

Regulatory record for Omnifit
Listed by Howmedica Osteonics Corp, United States
FDA product code JDI
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class Class 2
Regulation 21 CFR 888.3350
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
510(k) K913812
Record published 2015-09-24
Record revised 2026-07-24 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Lumen/inner diameter 22 to 32 mm

Catalogue Numbers

Catalogue numbers for Omnifit
Catalogue number Size Status
6088-0525-350L Stem Length: 350.0 Millimeter In distribution
J6097-0735 Neck Length: 35.0 Millimeter In distribution
6088-0730-350R Taper Connection: C-TPR In distribution
6098-0425 Stem Length: 100.0 Millimeter In distribution
6088-0730-350L Size: 7 In distribution
S-2302C-2850 Lumen/Inner Diameter 28.0 mm In distribution
1067-0011 Diameter: 11.0 Millimeter In distribution
6088-0730-200L Taper Connection: C-TPR In distribution
2041C-2648 Lumen/Inner Diameter 26.0 mm In distribution
6098-1040 Taper Connection: C-TPR In distribution
2043C-2274 Lumen/Inner Diameter 22.0 mm In distribution
2041C-3254 Lumen/Inner Diameter 32.0 mm In distribution
6088-0935-350R Taper Connection: C-TPR In distribution
6050-0735 Size: 7 In distribution
6088-0525-300L Stem Length: 300.0 Millimeter In distribution
J6098-0630 Neck Length: 30.0 Millimeter In distribution
2006-2644 Lumen/Inner Diameter 26.0 mm In distribution
6098-0835 Taper Connection: C-TPR In distribution
2041C-2654 Lumen/Inner Diameter 26.0 mm In distribution
2001-2844 Lumen/Inner Diameter 28.0 mm In distribution
J6097-1040 Taper Connection: V40? In distribution
1067-0018 Diameter: 18.0 Millimeter In distribution
2006-2252 Lumen/Inner Diameter 22.0 mm In distribution
J6098-0835 Size: 8 In distribution
6034-1240 Taper Connection: C-TPR In distribution
6088-0525-250L Stem Length: 250.0 Millimeter In distribution
J6097-0530 Size: 5 In distribution
6088-0730-250L Neck Length: 30.0 Millimeter In distribution
2001-3258 Lumen/Inner Diameter 32.0 mm In distribution
6070-0625A Taper Connection: C-TPR In distribution
6076-1035A Neck Length: 35.0 Millimeter In distribution
1067-0009 Diameter: 9.0 Millimeter In distribution
6098-0530 Taper Connection: C-TPR In distribution
J6097-0835 Neck Length: 35.0 Millimeter In distribution
6088-1140-250R Size: 11 In distribution
2043C-2646 Lumen/Inner Diameter 26.0 mm In distribution
6088-1140-200L Size: 11 In distribution
6098-1140 Size: 11 In distribution
6088-1140-300R Taper Connection: C-TPR In distribution
6088-0730-200R Stem Length: 200.0 Millimeter In distribution
2001-2652 Lumen/Inner Diameter 26.0 mm In distribution
6050-0745 Taper Connection: C-TPR In distribution
6017-1240A Stem Length: 170.0 Millimeter In distribution
6088-1140-350L Taper Connection: C-TPR In distribution
S-2302C-2862 Lumen/Inner Diameter 28.0 mm In distribution
2001-3261 Lumen/Inner Diameter 32.0 mm In distribution
6034-0525 Taper Connection: C-TPR In distribution
2006-2648 Lumen/Inner Diameter 26.0 mm In distribution
1067-0019 Diameter: 19.0 Millimeter In distribution
6050-0955 Taper Connection: C-TPR In distribution
2001-2240 Lumen/Inner Diameter 22.0 mm In distribution
2042C-2656 Lumen/Inner Diameter 26.0 mm In distribution
6097-0735 Taper Connection: C-TPR In distribution
6088-0935-200R Taper Connection: C-TPR In distribution
6088-0525-200L Taper Connection: C-TPR In distribution
2001-2852 Lumen/Inner Diameter 28.0 mm In distribution
2041C-2848 Lumen/Inner Diameter 28.0 mm In distribution
1067-0023 Diameter: 23.0 Millimeter In distribution
1067-0025 Diameter: 25.0 Millimeter In distribution
6033-0425 Stem Length: 100.0 Millimeter In distribution
J6098-0425 Size: 4 In distribution
2006-2861 Lumen/Inner Diameter 28.0 mm In distribution
1067-0008 Diameter: 8.0 Millimeter In distribution
1067-0022 Diameter: 22.0 Millimeter In distribution
J6098-0735 Size: 7 In distribution
J6097-0630 Neck Length: 30.0 Millimeter In distribution
6050-0935 Stem Length: 160.0 Millimeter In distribution
6088-0730-300L Stem Length: 300.0 Millimeter In distribution
2043C-2254 Lumen/Inner Diameter 22.0 mm In distribution
2001-2861 Lumen/Inner Diameter 28.0 mm In distribution
2001-2854 Lumen/Inner Diameter 28.0 mm In distribution
2001-3252 Lumen/Inner Diameter 32.0 mm In distribution
6050-1135 Taper Connection: C-TPR In distribution
6088-0525-300R Taper Connection: C-TPR In distribution
6088-0525-200R Size: 5 In distribution
6097-0630 Neck Length: 30.0 Millimeter In distribution
6088-1140-300L Stem Length: 300.0 Millimeter In distribution
6097-0425 Taper Connection: C-TPR In distribution
6097-0940 Neck Length: 40.0 Millimeter In distribution
2043C-3274 Lumen/Inner Diameter 32.0 mm In distribution
6097-1140 Taper Connection: C-TPR In distribution
2006-2244 Lumen/Inner Diameter 22.0 mm In distribution
2042C-2244 Lumen/Inner Diameter 22.0 mm In distribution
6097-1040 Taper Connection: C-TPR In distribution
6098-0940 Neck Length: 40.0 Millimeter In distribution
1067-0021 Diameter: 21.0 Millimeter In distribution
2001-2250 Lumen/Inner Diameter 22.0 mm In distribution
6088-0525-250R Stem Length: 250.0 Millimeter In distribution
1067-0013 Diameter: 13.0 Millimeter In distribution
J6098-0530 Taper Connection: V40? In distribution
6098-0735 Size: 7 In distribution
2001-3256 Lumen/Inner Diameter 32.0 mm In distribution
6097-0835 Size: 8 In distribution
6088-0935-350L Stem Length: 350.0 Millimeter In distribution
6088-0730-250R Size: 7 In distribution
S-2302C-3262 Lumen/Inner Diameter 32.0 mm In distribution
1067-0017 Diameter: 17.0 Millimeter In distribution
6033-0830 Taper Connection: C-TPR In distribution
1067-0016 Diameter: 16.0 Millimeter In distribution
6070-1035A Taper Connection: C-TPR In distribution
6076-0935A Taper Connection: C-TPR In distribution
6017-0425A Stem Length: 100.0 Millimeter In distribution
1067-0015 Diameter: 15.0 Millimeter In distribution
1067-0010 Diameter: 10.0 Millimeter In distribution
6034-0830 Size: 8 In distribution
6097-0530 Neck Length: 30.0 Millimeter In distribution
2042C-2648 Lumen/Inner Diameter 26.0 mm In distribution
6088-0935-250L Stem Length: 250.0 Millimeter In distribution
1067-0024 Diameter: 24.0 Millimeter In distribution
1067-0014 Diameter: 14.0 Millimeter In distribution
6017-1340A Stem Length: 170.0 Millimeter In distribution
2043C-2242 Lumen/Inner Diameter 22.0 mm In distribution
6088-0730-300R Size: 7 In distribution
6098-0630 Taper Connection: C-TPR In distribution
J6098-1040 Neck Length: 40.0 Millimeter In distribution
2001-2858 Lumen/Inner Diameter 28.0 mm In distribution
2041C-2240 Lumen/Inner Diameter 22.0 mm In distribution
6088-0935-250R Size: 9 In distribution
J6097-0425 Neck Length: 25.0 Millimeter In distribution
6088-0935-200L Neck Length: 35.0 Millimeter In distribution
6088-0525-350R Taper Connection: C-TPR In distribution
6088-1140-200R Stem Length: 200.0 Millimeter In distribution
6088-1140-250L Stem Length: 250.0 Millimeter In distribution
2001-2656 Lumen/Inner Diameter 26.0 mm In distribution
2001-2654 Lumen/Inner Diameter 26.0 mm In distribution
6033-0525 Size: 5 In distribution
2006-2248 Lumen/Inner Diameter 22.0 mm In distribution
6033-0935 Stem Length: 150.0 Millimeter In distribution
J6098-0940 Taper Connection: V40? In distribution
2001-2850 Lumen/Inner Diameter 28.0 mm In distribution
S-2301C-3258 Lumen/Inner Diameter 32.0 mm In distribution
6088-0935-300R Size: 9 In distribution
6034-1340 Stem Length: 170.0 Millimeter In distribution
S-2301C-3262 Lumen/Inner Diameter 32.0 mm In distribution
2041C-2858 Lumen/Inner Diameter 28.0 mm In distribution
2001-3250 Lumen/Inner Diameter 32.0 mm In distribution
6050-0530 Taper Connection: C-TPR In distribution
6050-0945 Taper Connection: C-TPR In distribution
6088-0935-300L Size: 9 In distribution
2043C-3250 Lumen/Inner Diameter 32.0 mm In distribution
1067-0012 Diameter: 12.0 Millimeter In distribution
S-2302C-3254 Lumen/Inner Diameter 32.0 mm In distribution
2042C-2252 Lumen/Inner Diameter 22.0 mm In distribution
2041C-2244 Lumen/Inner Diameter 22.0 mm In distribution
J6097-0940 Neck Length: 40.0 Millimeter In distribution
6017-0625A Stem Length: 120.0 Millimeter In distribution
2001-2258 Lumen/Inner Diameter 22.0 mm In distribution
1067-0020 Diameter: 20.0 Millimeter In distribution
6088-1140-350R Stem Length: 350.0 Millimeter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Zimmer, Inc. 836
R3 Smith & Nephew, Inc. 497
UniSyn Hip System Shalby Advanced Technologies, Inc. 247
UniSyn® Hip System Consensus Orthopedics, Inc. 247
Reflection Smith & Nephew, Inc. 170
Instrument Howmedica Osteonics Corp 167
Echelon Smith & Nephew, Inc. 159
B-P Total HIP System Endotec, Inc. 151
ZCA® Zimmer, Inc. 149
Ringloc HIP System Biomet Orthopedics 139
Profemur Microport Orthopedics Inc. 113
OSS™ Orthopedic Salvage System Biomet Orthopedics 98

Showing 12 of 444. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K193429 2020-08-13
K120578 2012-03-29
K110290 2011-09-27
K052748 2005-12-02
K051363 2005-06-23
K050138 2005-03-21
K031730 2003-08-29
K031744 2003-08-08
K022799 2002-11-21
K022077 2002-07-25
K021310 2002-05-21
K020989 2002-04-26
K012026 2001-07-18
K011623 2001-06-15
K010757 2001-04-11
K010310 2001-03-20
K001956 2000-12-11

Recalls Naming This Product

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

Recalls naming the identifiers of Omnifit
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Howmedica Osteonics Corp 510(k) number 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
Howmedica Osteonics Corp 510(k) number 2019-11-07 Class II Employee error May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire 20 units 2020-08-31
Howmedica Osteonics Corp 510(k) number 2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
Howmedica Osteonics Corp 510(k) number 2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
Howmedica Osteonics Corp 510(k) number 2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
Howmedica Osteonics Corp 510(k) number 2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
Howmedica Osteonics Corp 510(k) number 2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20
Howmedica Osteonics Corp 510(k) number 2008-11-13 Not classified Packaging Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices. 322 total units – all types 2010-01-20

Recalls

17 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
2025-08-28 Class II Under Investigation by firm a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted. 55 units (all OUS)
2024-08-05 Class II Process control A patient specific, custom-made device was supplied for a surgical procedure that did not match the design proposal. 1 unit (OUS only)
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2018-05-22 Class II Process control The recalling firm has received a higher than expected number of complaints documenting femoral head/hip stem disassociation for certain sizes of femoral heads manufactured prior to March 4, 2011. 2020-05-08
2016-08-29 Class II Under Investigation by firm Stryker received several complaints describing incidence of harm secondary to taper lock failure for specific lots of numerous catalog numbers of LFIT Anatomic CoCr V40 Femoral Heads. 42,519 units (total Catalog numbers) 2017-05-02
2016-07-01 Class II Device Design Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle. 241 units 2017-06-08
2015-10-15 Class II Under Investigation by firm Six (6) PCA 10 Degree Hooded Acetabular Insert-Duration 22 mm (ID) have been distributed in the US, although the 22 mm size was inadvertently omitted from 510(k) #K963612. 1 unit 2017-06-08
2015-02-03 Class II Under Investigation by firm Three customer complaints were received for the same batch of V40 LFIT Vitallium femoral heads (part number 6260-9-032, lot 48681201) alleging that the femoral head couldn’t be assembled with its corresponding V40 stem trunnion. 9 units 2017-04-07
2013-10-25 Class II Packaging process control Stryker received a report from the field indicating that an Accolade II Hip Stem Size #3 was identified in packaging with an Accolade II Hip Stem Size #5. 20 units 2015-03-31
2012-07-16 Class II Device Design Stryker has become aware that insufficient taper torsional strength may result when a PAR extension piece is used with a forged CoCr stem. 301 units 2015-09-09
2011-12-29 Class II Employee error Stryker Orthopaedics has become aware of the potential for cracking of the PMMA coating on their PM COCR Hip Stem product. 16,913 units 2015-03-19
2010-03-31 Not classified Process control One lot of 13 mm medium distal ring centralizers and 14 mm large distal ring centralizer have been labeled incorrectly. The size 14 Large centralizers have been labeled as size 13 Medium centralizers and size 13 Medium centralizers have bee 17 2010-07-09
2010-03-31 Not classified Process control One lot of 13 mm medium distal ring centralizers and 14 mm large distal ring centralizer have been labeled incorrectly. The size 14 Large centralizers have been labeled as size 13 Medium centralizers and size 13 Medium centralizers have bee 15 2010-07-09
2010-03-29 Not classified Error in labeling Stryker became aware that device labels have incorrectly printed manufacture dates and thus incorrect expiration dates on the product label. 24 units 2012-09-10
2007-12-18 Not classified Labeling design The GMRS Proximal Femoral Surgical Protocol states ” The GMRS Proximal Femoral components are fully compatabile with all Stryker V40 femoral heads.” This statement is incorrect and conflicts with the Alumina Head label and packaging insert 5869 2008-10-15
2007-11-15 Not classified Process design Curvature Discrepancy –The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy –The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-15 Not classified Process design Curvature Discrepancy — The radius of curvature may be out of specification to varying degrees causing a discrepency in the stem curvature between trials and implants. 803 total, all sizes 2008-09-22
2007-11-02 Not classified Other Fracture of Stem Neck – The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in p 5,599 total units 2010-08-30
2007-11-02 Not classified Other Fracture of Stem Neck – The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in p 5,599 total units 2010-08-30
2007-11-02 Not classified Other Fracture of Stem Neck – The firm recently performed laboratory testing indicates that there may be a potential increased risk of stem neck fractures when a V40 +16mm offset femoral head is mated with certain Accolade TMZF femoral stems in p 5,599 total units 2010-08-30

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