REVO C6101A
GUDID 10845854015070
REVO SCREW PRELOADED
Conmed Corporation
Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable| Primary Device ID | 10845854015070 |
| NIH Device Record Key | d2d0d85e-530d-468d-b4ba-2afaa360cfa3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REVO |
| Version Model Number | C6101A |
| Catalog Number | C6101A |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854015070 [Primary] |
| GS1 | 20845854015077 [Package] Package: Box [1 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K963932
FDA Product Code
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2024-01-11 |
| Device Publish Date | 2015-10-24 |
On-Brand Devices [REVO]
| 20845854019792 | 4MM REVO ANCHOR, PRETHREADED, TWO No. 2 (5 METRIC) HI-FI |
| 20845854019785 | 4MM REVO ANCHOR, PRETHREADED, No. 2 (5 METRIC) HI-FI |
| 10845854026717 | Thin Shaft Revo Driver |
| 20845854030759 | MINI-REVO DRILL, 1.5MM |
| 20845854030834 | MINI-REVO TAP |
| 20845854030742 | MINI-REVO BONE PUNCH 1.5MM |
| 20845854030728 | MINI-REVO DRIVER |
| 20845854030704 | 2MM REVO BONE PUNCH |
| 20845854030674 | REVO CROCHET HOOK |
| 30845854030763 | MINI-REVO DRILL GUIDE, 1.5MM |
| 10845854015070 | REVO SCREW PRELOADED |
Trademark Results [REVO]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 REVO 98594149 not registered Live/Pending |
IterationX Inc. 2024-06-10 |
 REVO 98543874 not registered Live/Pending |
Tim Koehler 2024-05-10 |
 REVO 98444755 not registered Live/Pending |
MEGAMESH INTERNATIONAL LIMITED 2024-03-12 |
 REVO 98401269 not registered Live/Pending |
Revo Holdings, LLC 2024-02-11 |
 REVO 98292812 not registered Live/Pending |
Revo S.A. 2023-11-30 |
 REVO 98209981 not registered Live/Pending |
RAIN Scientific, Inc. 2023-10-04 |
 REVO 98133301 not registered Live/Pending |
General Maven 2023-08-15 |
 REVO 97902530 not registered Live/Pending |
Natures Gold Reserve Inc. 2023-04-23 |
 REVO 97492285 not registered Live/Pending |
KAYHAN AV TÃFEKLERI SANAYI VE DIS TICARET LIMITED SIRKETI 2022-07-07 |
 REVO 97323954 not registered Live/Pending |
Revo Design, LLC 2022-03-22 |
 REVO 97142314 not registered Live/Pending |
REVO Group, LLC 2021-11-24 |
 REVO 97142307 not registered Live/Pending |
REVO Group, LLC 2021-11-24 |
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