RingLoc® Hip System 12-105994
GUDID 00887868342790
Biomet Orthopedics, LLC
Non-constrained polyethylene acetabular liner| Primary Device ID | 00887868342790 |
| NIH Device Record Key | d7421504-ea5d-4124-a1b1-1803b86c2cc9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RingLoc® Hip System |
| Version Model Number | 12-105994 |
| Catalog Number | 12-105994 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 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 | 00887868342790 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K032396
FDA Product Code
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-26 |
| Device Publish Date | 2019-04-18 |
On-Brand Devices [RingLoc® Hip System]
| 00887868343223 | XL-195238 |
| 00887868343216 | XL-195237 |
| 00887868343209 | XL-195236 |
| 00887868343193 | XL-195235 |
| 00887868343186 | XL-195234 |
| 00887868343087 | XL-106998 |
| 00887868343070 | XL-106997 |
| 00887868343063 | XL-106996 |
| 00887868343056 | XL-106995 |
| 00887868343049 | XL-106988 |
| 00887868343032 | XL-106987 |
| 00887868343025 | XL-106986 |
| 00887868343018 | XL-106985 |
| 00887868342837 | 12-105998 |
| 00887868342820 | 12-105997 |
| 00887868342813 | 12-105996 |
| 00887868342806 | 12-105995 |
| 00887868342790 | 12-105994 |
| 00887868359361 | 11-105900 |
| 00887868348020 | EP-156233 |
| 00887868348013 | EP-155232 |
| 00887868348006 | EP-105951 |
| 00887868347993 | EP-105790 |
| 00887868347986 | EP-105780 |
| 00887868230066 | 105428 |
| 00887868230059 | 105427 |
| 00887868230042 | 105426 |
| 00887868230035 | 105425 |
| 00887868230028 | 105424 |
| 00887868230011 | 105423 |
| 00887868230004 | 105422 |
| 00887868229992 | 105421 |
| 00887868229985 | 105420 |
Trademark Results [RingLoc]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RINGLOC 75014549 not registered Dead/Abandoned |
Aesculap AG 1995-11-03 |
 RINGLOC 74307357 1811999 Live/Registered |
Biomet Manufacturing, LLC 1992-08-24 |
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