REDUX 014599
GUDID 03596010381583
9MM METAL ACL OBTURATOR
Smith & Nephew, Inc.
Surgical drill guide obturator| Primary Device ID | 03596010381583 |
| NIH Device Record Key | a9ad0301-038a-4b1a-9ccd-68c720e593fe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REDUX |
| Version Model Number | 014599 |
| Catalog Number | 014599 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, 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 | false |
| 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 |
Customer Support Contacts
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03596010381583 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K932718
FDA Product Code
| HRX | ARTHROSCOPE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
[03596010381583]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2015-08-30 |
On-Brand Devices [REDUX]
| 00885556539163 | WAVE WASHER |
| 03596010381637 | EXTRACTOR SCREW ACL REDUX |
| 03596010381620 | RETAINER SCREW ACL REDUX |
| 03596010381699 | TRAY ACL REDUX STERILIZATION |
| 03596010381682 | DRIVER ACL REDUX-3.4MM |
| 03596010381675 | DRIVER ACL REDUX-2.7MM |
| 03596010381668 | DRIVER ACL REDUX-2.4MM |
| 03596010381651 | DRIVER ACL REDUX-2.3MM |
| 03596010381644 | DRIVER ACL REDUX-1.9MM |
| 03596010381613 | ACL REDUX BONE PIC |
| 03596010381606 | ACL REDUX TM RASP PICK |
| 03596010381583 | 9MM METAL ACL OBTURATOR |
| 03596010381576 | 9MM METAL ACL CANNULA |
| 03596010381569 | HDL UNIVERSAL ACL REDUX |
| 03596010026071 | 10MM METAL ACL OBTURATOR |
| 03596010026057 | 10MM METAL ACL CANNULA |
Trademark Results [REDUX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 REDUX 98323823 not registered Live/Pending |
West Coast Reduction Ltd. 2023-12-20 |
 REDUX 97414674 not registered Live/Pending |
Smith & Wesson Inc. 2022-05-17 |
 REDUX 97250657 not registered Live/Pending |
Elevated Solutions 512Group Holdings LLC 2022-02-02 |
 REDUX 97140107 not registered Live/Pending |
Lost Girl Beauty LLC 2021-11-23 |
 REDUX 97135995 not registered Live/Pending |
Training For Climbing, LLC 2021-11-21 |
 REDUX 88889043 not registered Live/Pending |
HANAPS ENTERPRISES 2020-04-27 |
 REDUX 88797134 not registered Live/Pending |
Yurick, Sean M 2020-02-13 |
 REDUX 88770640 not registered Live/Pending |
Good News Productions International 2020-01-23 |
 REDUX 88564107 not registered Live/Pending |
Revive Electronics 2019-08-02 |
 REDUX 88453412 not registered Live/Pending |
VOC Ventures 2019-05-30 |
 REDUX 87809257 5704893 Live/Registered |
Bentley Mills, Inc. 2018-02-23 |
 REDUX 87598971 not registered Dead/Abandoned |
Zimmer Biomet Spine, Inc. 2017-09-07 |
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