Arthrex®
- Primary DI
- 00888867304604
- Brand
- Arthrex®
- Company
- ARTHREX, INC.
- Model
- AR-7286
- Catalog number
- AR-7286
- Device description
- FiberButton, Oval 14mm x 8mm
- Published
- 2026-07-08
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MAI | Fastener, fixation, biodegradable, soft tissue |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAI | Fastener, Fixation, Biodegradable, Soft Tissue | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10888867304601 | Package | GS1 | 5 | In Commercial Distribution |
| 00888867304604 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10888867304601 | 10888867304601 | ||
| 00888867304604 | 00888867304604 | 888867304604 | 0888867304604 |
GMDN Terms#
| Term | Definition |
|---|---|
| Tendon/ligament bone anchor, non-bioabsorbable | A non-bioabsorbable device designed to be implanted into bone for the attachment of tendons/ligaments/soft tissues either directly or via a suture attached to the device; typically used in arthroscopic or open surgical procedures. This device is available in various designs and sizes and is made of a material that cannot be chemically degraded or absorbed via natural body processes [e.g., titanium (Ti)]. |
Contacts#
| Phone | |
|---|---|
| +1(800)934-4404 | complaints@arthrex.com |
Regulatory Flags#
- DUNS number
- 131747628
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888867576032 | Arthrex® | AR-3636-REMP | AR-3636-REMP | 2026-10-20 |
| 00888867576056 | Arthrex® | AR-3641SP-REMP | AR-3641SP-REMP | 2026-10-20 |
| 00888867576070 | Arthrex® | AR-6573-1 | AR-6573-1 | 2026-10-20 |
| 00888867576087 | Arthrex® | AR-6573-2 | AR-6573-2 | 2026-10-20 |
| 00888867568280 | Arthrex® | AR-3210-0050-SJ | AR-3210-0050-SJ | 2026-10-16 |
| 00888867568297 | Arthrex® | AR-3210-0051-SJ | AR-3210-0051-SJ | 2026-10-16 |
| 00888867568303 | Arthrex® | AR-3210-0059-PK | AR-3210-0059-PK | 2026-10-16 |
| 00888867568310 | Arthrex® | AR-3210-0063-PK | AR-3210-0063-PK | 2026-10-16 |
| 00888867568457 | Arthrex® | AR-8650DS-N | AR-8650DS-N | 2026-10-16 |
| 00888867427143 | Arthrex® | AR-S6524-025-230C | AR-S6524-025-230C | 2023-06-05 |
| 00888867389533 | Arthrex® | AR-9928BCK-MIS | AR-9928BCK-MIS | 2023-05-22 |
| 00888867276086 | Arthrex® | AR-9437-16 | AR-9437-16 | 2022-07-15 |
| 00888867060401 | Arthrex® | AR-9439-16 | AR-9439-16 | 2018-06-02 |
| 00888867060418 | Arthrex® | AR-9439-18 | AR-9439-18 | 2018-06-02 |
| 00888867060425 | Arthrex® | AR-9441-16 | AR-9441-16 | 2018-06-14 |
| 00888867060432 | Arthrex® | AR-9441-18 | AR-9441-18 | 2018-06-02 |
| 00888867060449 | Arthrex® | AR-9443-16 | AR-9443-16 | 2018-06-14 |
| 00888867060456 | Arthrex® | AR-9443-18 | AR-9443-18 | 2018-06-14 |
| 00888867060463 | Arthrex® | AR-9445-17 | AR-9445-17 | 2018-06-28 |
| 00888867060470 | Arthrex® | AR-9445-19 | AR-9445-19 | 2018-06-02 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00888867627840 | Arthrex® | ARTHREX, INC. | MAI | 2026-10-07 |
| 00888867627857 | Arthrex® | ARTHREX, INC. | MAI | 2026-10-07 |
| 00888867627864 | Arthrex® | ARTHREX, INC. | MAI | 2026-10-07 |
| 20845854655501 | Argo Knotless | Conmed Corporation | MAI | 2026-09-25 |
| 20653405990908 | GENESYS™ CrossFT™ | Conmed Corporation | MAI | 2026-07-31 |
| 20653405990915 | GENESYS™ CrossFT™ | Conmed Corporation | MAI | 2026-07-31 |
| 20653405990922 | GENESYS™ CrossFT™ | Conmed Corporation | MAI | 2026-07-31 |
| 20653405990939 | GENESYS™ CrossFT™ | Conmed Corporation | MAI | 2026-07-31 |
| 20653405990946 | GENESYS™ CrossFT™ | Conmed Corporation | MAI | 2026-07-31 |
| 20653405990953 | GENESYS™ CrossFT™ | Conmed Corporation | MAI | 2026-07-31 |
| 07290019361206 | OSSIOfiber® Interference Screw | OSSIO LTD | MAI | 2026-07-19 |
| 07290019361213 | OSSIOfiber® Interference Screw | OSSIO LTD | MAI | 2026-07-19 |
| 07290019361220 | OSSIOfiber® Interference Screw | OSSIO LTD | MAI | 2026-07-19 |
| 00888867304598 | Arthrex® | ARTHREX, INC. | MAI | 2026-07-08 |
| 00888867304789 | Arthrex® | ARTHREX, INC. | MAI | 2026-07-08 |
| 00888867304796 | Arthrex® | ARTHREX, INC. | MAI | 2026-07-08 |
| 00816537023012 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00816537023029 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00816537023036 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00816537023043 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00816537023050 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00816537023067 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00816537023234 | FiberFIX | NANOVA BIO MATERIALS INC | MAI | 2026-06-09 |
| 00888867483927 | Arthrex® | ARTHREX, INC. | MAI | 2025-11-06 |
| 07649990202174 | Geomax Reamer S-PI-A1.6 | Surgical Fusion Technologies GmbH | MAI | 2025-10-01 |
| 07649990202211 | Geomax Reamer S-PI-A2.3 | Surgical Fusion Technologies GmbH | MAI | 2025-10-01 |
| 07613327662016 | KNOTILUS+ | STRYKER CORPORATION | MAI | 2025-06-16 |
| 07613327662030 | ALPHAVENT | STRYKER CORPORATION | MAI | 2025-06-16 |
| 07613327662047 | ALPHAVENT | STRYKER CORPORATION | MAI | 2025-06-16 |
| 07613327662054 | ALPHAVENT | STRYKER CORPORATION | MAI | 2025-06-16 |