Cohere
GUDID 00887517020734
COHERE TLIF-O, 10x10x25mm 4°
Nuvasive, Inc.
Polymeric spinal interbody fusion cage| Primary Device ID | 00887517020734 |
| NIH Device Record Key | e2c75d98-d533-44b0-b3a8-b88efdcad1f5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cohere |
| Version Model Number | 6100254P2 |
| Company DUNS | 053950783 |
| Company Name | Nuvasive, 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 | true |
| 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
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517020734 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K193541
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
[00887517020734]
Radiation Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-23 |
| Device Publish Date | 2021-06-15 |
On-Brand Devices [Cohere]
| 00887517982841 | COHERE XL, 12x18x55mm 10° |
| 00887517982827 | COHERE XL, 12x18x50mm 10° |
| 00887517982766 | COHERE XL, 10x18x55mm 10° |
| 00887517982742 | COHERE XL, 10x18x50mm 10° |
| 00887517982681 | COHERE XL, 8x18x55mm 10° |
| 00887517982667 | COHERE XL, 8x18x50mm 10° |
| 00887517983329 | COHERE XLW, 12x22x55mm 10° |
| 00887517983305 | COHERE XLW, 12x22x50mm 10° |
| 00887517983244 | COHERE XLW, 10x22x55mm 10° |
| 00887517983220 | COHERE XLW, 10x22x50mm 10° |
| 00887517983169 | COHERE XLW, 8x22x55mm 10° |
| 00887517983145 | COHERE XLW, 8x22x50mm 10° |
| 00887517982360 | COHERE XLW, 12x22x55mm 15° |
| 00887517982346 | COHERE XLW, 12x22x50mm 15° |
| 00887517982285 | COHERE XLW, 10x22x55mm 15° |
| 00887517982261 | COHERE XLW, 10x22x50mm 15° |
| 00887517982209 | COHERE XLW, 8x22x55mm 15° |
| 00887517982186 | COHERE XLW, 8x22x50mm 15° |
| 00887517943538 | COHERE Tamp, Assembly HS |
| 00887517025937 | Alpha Cohere TLIF-O Core Instrument Set |
| 00887517014047 | COHERE TLIF-O Trial, 16x10mm 12° |
| 00887517014023 | COHERE TLIF-O Trial, 14x14mm 4° |
| 00887517014016 | COHERE TLIF-O Trial, 14x10mm 12° |
| 00887517014009 | COHERE TLIF-O Trial, 14x10mm 4° |
| 00887517013255 | COHERE TLIF-O Inserter, 14mm |
| 00887517013248 | COHERE TLIF-O Inserter, 10x30-35mm |
| 00887517013231 | COHERE TLIF-O Inserter, 10x25mm |
| 00887517013187 | COHERE TLIF-O Trial, 12x14mm 4° |
| 00887517013170 | COHERE TLIF-O Trial, 12x10mm 12° |
| 00887517013163 | COHERE TLIF-O Trial, 12x10mm 4° |
| 00887517013156 | COHERE TLIF-O Trial, 11x10mm 8° |
| 00887517013149 | COHERE TLIF-O Trial, 10x14mm 4° |
| 00887517013125 | COHERE TLIF-O Trial, 10x10mm 4° |
| 00195377028150 | COHERE TLIF-O Trial, 12x10mm 8° |
| 00195377028143 | COHERE TLIF-O Trial, 14x10mm 8° |
| 00195377028136 | COHERE TLIF-O Trial, 16x10mm 4° |
| 00195377028129 | COHERE TLIF-O Trial, 16x10mm 8° |
| 00195377028112 | COHERE TLIF-O Trial, 18x10mm 8° |
| 00195377028105 | COHERE TLIF-O Trial, 18x10mm 12° |
| 00887517984067 | COHERE XLXW, 8x26x60mm 0° |
| 00887517984043 | COHERE XLXW, 8x26x55mm 0° |
| 00887517984029 | COHERE XLXW, 8x26x50mm 0° |
| 00887517984005 | COHERE XLXW, 8x26x45mm 0° |
| 00887517983985 | COHERE XLXW, 12x26x60mm 0° |
| 00887517983961 | COHERE XLXW, 12x26x55mm 0° |
| 00887517983947 | COHERE XLXW, 12x26x50mm 0° |
| 00887517983923 | COHERE XLXW, 12x26x45mm 0° |
| 00887517983909 | COHERE XLXW, 10x26x60mm 0° |
| 00887517983886 | COHERE XLXW, 10x26x55mm 0° |
| 00887517983862 | COHERE XLXW, 10x26x50mm 0° |
Trademark Results [Cohere]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COHERE 98478957 not registered Live/Pending |
COHERE INC. 2024-04-01 |
 COHERE 98001871 not registered Live/Pending |
COHERE INC. 2023-05-18 |
 COHERE 97543315 not registered Live/Pending |
COHERE INC. 2022-08-10 |
 COHERE 97368784 not registered Live/Pending |
Cohere Life, Inc. 2022-04-18 |
 COHERE 97368545 not registered Live/Pending |
Cohere Life, Inc. 2022-04-18 |
 COHERE 90723898 not registered Live/Pending |
COHERE INC. 2021-05-20 |
 COHERE 88980207 not registered Live/Pending |
COHERE INC. 2019-05-29 |
 COHERE 88792403 not registered Live/Pending |
Cambia Health Solutions, Inc. 2020-02-11 |
 COHERE 88785526 not registered Live/Pending |
Cohere Capital Partners, LP 2020-02-05 |
 COHERE 88450483 not registered Live/Pending |
Paul Oran 2019-05-29 |
 COHERE 88273838 not registered Live/Pending |
Humans First Detroit 2019-01-23 |
 COHERE 87921611 not registered Live/Pending |
Corporate Concierge Services, Inc. 2018-05-15 |
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