Converge®
GUDID 00889024170698
Zimmer, Inc.
Acetabular shell| Primary Device ID | 00889024170698 |
| NIH Device Record Key | ae5a5caa-53af-47d0-8981-0dd9a6041300 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Converge® |
| Version Model Number | 5360-00-061 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024170698 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K012739
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 | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-17 |
On-Brand Devices [Converge®]
Trademark Results [Converge]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CONVERGE 98749112 not registered Live/Pending |
The Brebet Company LLC 2024-09-13 |
 CONVERGE 98627741 not registered Live/Pending |
LLC YTCC 2024-07-01 |
 CONVERGE 98501002 not registered Live/Pending |
Converge Direct, LLC 2024-04-15 |
 CONVERGE 98185818 not registered Live/Pending |
ENEN GROUP LIMITED 2023-09-19 |
 CONVERGE 98035327 not registered Live/Pending |
Converge Inc. 2023-06-09 |
 CONVERGE 97921179 not registered Live/Pending |
Chiu, Connor 2023-05-04 |
CONVERGE 97921179 not registered Live/Pending |
Alba, Christopher 2023-05-04 |
 CONVERGE 97824615 not registered Live/Pending |
PACKETFABRIC, INC. 2023-03-06 |
 CONVERGE 97699486 not registered Live/Pending |
Circle Internet Financial Limited 2022-12-01 |
 CONVERGE 97436429 not registered Live/Pending |
Verge Analytics, Inc. 2022-05-31 |
 CONVERGE 97224362 not registered Live/Pending |
Anthony Dagostino 2022-01-18 |
 CONVERGE 97174238 not registered Live/Pending |
SK Converge S.A. 2021-12-15 |
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