| Primary Device ID | 10381780527343 |
| NIH Device Record Key | 134f3cdf-b77a-4bd5-96da-c02f96ef4760 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CADENCE® |
| Version Model Number | 10200102 |
| Catalog Number | 10200102 |
| Company DUNS | 942377524 |
| Company Name | Ascension Orthopedics, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Special Storage Condition, Specify | Between 0 and 0 *Do Not Use If Package Is Damaged |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10381780527343 [Primary] |
| LHX | Trousers, anti-shock |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-08 |
| Device Publish Date | 2020-11-30 |
| 10381780417132 | 45° Tibial Impactor Tip |
| 10381780417125 | Module for Pins, Drivers, and Accessories |
| 10381780417118 | Size 5 Tibial Trial - Left |
| 10381780417101 | Size 4X Tibial Trial - Left |
| 10381780417095 | Size 4 Tibial Trial - Left |
| 10381780417088 | Size 3X Tibial Trial - Left |
| 10381780417071 | Size 3 Tibial Trial - Left |
| 10381780417064 | Size 2X Tibial Trial - Left |
| 10381780417057 | Size 2 Tibial Trial - Left |
| 10381780417040 | Size 1X Tibial Trial - Left |
| 10381780417033 | Size 1 Tibial Trial - Left |
| 10381780417026 | Size 5 Tibial Trial - Right |
| 10381780417019 | Size 4X Tibial Trial - Right |
| 10381780417002 | Size 4 Tibial Trial - Right |
| 10381780416999 | Size 3X Tibial Trial - Right |
| 10381780416982 | Size 3 Tibial Trial - Right |
| 10381780416975 | Size 2X Tibial Trial - Right |
| 10381780416968 | Size 2 Tibial Trial - Right |
| 10381780416951 | Size 1X Tibial Trial - Right |
| 10381780416944 | Size 1 Tibial Trial - Right |
| M248CADENCERESECT1 | Cadence Total Ankle Resection Instruments |
| M248CADENCEINSERT1 | Cadence Trials, Insertion, and Removal Instruments |
| M248CADENCERESECT121 | Cadence Total Ankle Resection Instruments |
| M248CADENCEINSERT121 | Cadence Trials, Insertion, and Removal Instruments |
| 10381780530176 | Surgical Instruments, Generic Case Lid Half Size |
| 10381780530169 | Cadence®Total Ankle System, Case, Cadence Flat Cut Instruments, Alternate |
| 10381780530152 | Cadence®Total Ankle System, Case, Cadence Flat Cut Instruments |
| 10381780527350 | Cadence®Total Ankle System, Talar Flat Cut Guide |
| 10381780527343 | Cadence®Total Ankle System, 2mm Talar Cut Guide |
| 10381780527336 | Cadence®Total Ankle System, Talar Flat Cut Drill Guide |
| 10381780527329 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 5, Left |
| 10381780527312 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 4, Left |
| 10381780527305 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 3, Left |
| 10381780527299 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 2, Left |
| 10381780527282 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 1, Left |
| 10381780527268 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 5, Right |
| 10381780527251 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 4, Right |
| 10381780527244 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 3, Right |
| 10381780527237 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 2, Right |
| 10381780527220 | Cadence®Total Ankle System, Flat Cut Talar Trial, Size 1, Right |
| 10381780527206 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 5, Left |
| 10381780527190 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 4, Left |
| 10381780527183 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 3, Left |
| 10381780527176 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 2, Left |
| 10381780527169 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 1, Left |
| 10381780527145 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 5, Right |
| 10381780527138 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 4, Right |
| 10381780527121 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 3, Right |
| 10381780527114 | Cadence®Total Ankle System, Flat Cut Talar Dome, Size 2, Right |
| 10381780527107 | Cadence® Total Ankle System, Flat Cut Talar Dome, Size 1, Right |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CADENCE 98868109 not registered Live/Pending |
Baby Delight, Inc. 2024-11-22 |
![]() CADENCE 98751672 not registered Live/Pending |
Gallagher Fragrances LLC 2024-09-15 |
![]() CADENCE 98549200 not registered Live/Pending |
SEMO 2024-05-14 |
![]() CADENCE 98524508 not registered Live/Pending |
Tempo Together, Inc. 2024-04-29 |
![]() CADENCE 98512565 not registered Live/Pending |
KEEP YOUR CADENCE, INC. 2024-04-22 |
![]() CADENCE 98478252 not registered Live/Pending |
Impact Foods Inc. 2024-04-01 |
![]() CADENCE 98375586 not registered Live/Pending |
Wilson Sporting Goods Co. 2024-01-25 |
![]() CADENCE 98321305 not registered Live/Pending |
Cadence Performance, Inc. 2023-12-19 |
![]() CADENCE 98157787 not registered Live/Pending |
BARS AI, INC. 2023-08-30 |
![]() CADENCE 97978759 not registered Live/Pending |
Cadence Solutions, Inc. 2022-08-24 |
![]() CADENCE 97768154 not registered Live/Pending |
Mackay Family Trust 2023-01-25 |
![]() CADENCE 97768149 not registered Live/Pending |
Mackay Family Trust 2023-01-25 |