Oxford® 32-423030
GUDID 00887868485121
Biomet Orthopedics, LLC
Knee femur prosthesis trial| Primary Device ID | 00887868485121 |
| NIH Device Record Key | 93f543f0-da2a-487a-875c-5f0e413966fd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Oxford® |
| Version Model Number | 32-423030 |
| Catalog Number | 32-423030 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868485121 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K133940
FDA Product Code
| HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
[00887868485121]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-12 |
| Device Publish Date | 2021-04-02 |
On-Brand Devices [Oxford®]
Trademark Results [Oxford]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 OXFORD 98385249 not registered Live/Pending |
Baney Corporation 2024-01-31 |
 OXFORD 98100221 not registered Live/Pending |
Strong Industries, Inc. 2023-07-25 |
 OXFORD 98068223 not registered Live/Pending |
ozar gonzalez, jefferson j 2023-07-01 |
 OXFORD 97721471 not registered Live/Pending |
Oxford Holding Company, LLC 2022-12-16 |
 OXFORD 97720833 not registered Live/Pending |
The Oxford Asset Management Company Limited 2022-12-16 |
 OXFORD 88945617 not registered Live/Pending |
K. Hansotia & Co., Inc. 2020-06-03 |
 OXFORD 88304116 not registered Live/Pending |
Oxford Porcelanas S/A 2019-02-15 |
 OXFORD 87920461 not registered Dead/Abandoned |
ND PAPER LLC 2018-05-14 |
 OXFORD 87750435 not registered Live/Pending |
OPGI Management GP Inc./Gestion OPGI GPInc., as general partner for OPGI Management Limited Partnership 2018-01-10 |
 OXFORD 87689938 5469769 Live/Registered |
Oxford Products USA, Inc. 2017-11-17 |
 OXFORD 87672968 5486551 Live/Registered |
Oxford Products USA, Inc. 2017-11-06 |
 OXFORD 87534558 5396286 Live/Registered |
Oxford Insurance Group, Inc. 2017-07-19 |
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