BENDER
- Primary DI
- 00888118090225
- Brand
- BENDER
- Company
- KLS-Martin L.P.
- Model
- 96-300-76-07
- Published
- 2018-09-26
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| HXW | BENDER |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| HXW | Bender | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118090225 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118090225 | 00888118090225 | 888118090225 | 0888118090225 |
GMDN Terms
| Term | Definition |
|---|---|
| Bone fixation plate pliers | A manual surgical instrument designed to bend and cut light-bone fixation plates (e.g., 1 to 2 mm in thickness), such as those used in craniomaxillofacial (CMF) or finger surgery. The instrument is typically made of high-grade steel and consists of two arms/rods that form a handle proximally and extend distally through a pivot to form jaws that bend and cut the metal plates allowing the surgeon to customize their size and shape. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(904)641-7746 | KLS-UDI-Info@klsmartin.com |
Regulatory Flags
- DUNS number
- 826499238
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888118131782 | LEVEL ONE EXTREMITY | 26-066-60-09 | 2026-05-25 | |
| 00888118131799 | LEVEL ONE EXTREMITY | 26-066-70-09 | 2026-05-25 | |
| 00888118144928 | LEVEL ONE EXTREMITY | 26-950-40-07 | 2026-05-25 | |
| 00888118145284 | PURE PECTUS | 24-070-60-09 | 2026-05-25 | |
| 00888118145291 | PURE PECTUS | 24-070-62-09 | 2026-05-25 | |
| 00888118150240 | PURE PECTUS | CTM-241-100-01 | 2026-05-25 | |
| 00888118150257 | PURE PECTUS | CTM-241-101-01 | 2026-05-25 | |
| 00888118150264 | PURE PECTUS | CTM-241-200-01 | 2026-05-25 | |
| 00888118150448 | IXOS | CTM-263-100-01 | 2026-05-25 | |
| 00888118150455 | IXOS | CTM-263-101-01 | 2026-05-25 | |
| 00888118150462 | IXOS | CTM-263-202-01 | 2026-05-25 | |
| 00888118150479 | IXOS | CTM-263-202-02 | 2026-05-25 | |
| 00888118150486 | IXOS | CTM-263-202-03 | 2026-05-25 | |
| 00888118150493 | IXOS | CTM-263-202-04 | 2026-05-25 | |
| 00888118150646 | IPS | 60-011-42-09-LP | 2026-05-25 | |
| 00888118153029 | L1 STERNAL | CTM-242-302-01 | 2026-05-25 | |
| 00888118153050 | IXOS | CTM-263-203-01 | 2026-05-25 | |
| 00888118153067 | IXOS | CTM-263-203-02 | 2026-05-25 | |
| 00888118153074 | IXOS | CTM-263-203-03 | 2026-05-25 | |
| 00888118153081 | IXOS | CTM-263-203-04 | 2026-05-25 |
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| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00888118144928 | LEVEL ONE EXTREMITY | KLS-Martin L.P. | HXW | 2026-05-25 |
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| 00840536800237 | Response Spine System | ORTHOPEDIATRICS CORP. | HXW | 2026-01-15 |
| 00840180543283 | General Instruments | ALPHATEC SPINE, INC. | HXW | 2025-12-31 |
| 00840180543290 | General Instruments | ALPHATEC SPINE, INC. | HXW | 2025-12-31 |
| 10889981095987 | General | Seaspine Orthopedics Corporation | HXW | 2025-12-19 |
| 03662663261869 | BacFix Ti Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-12-18 |
| 00840194418140 | Pediflex | ORTHOPEDIATRICS CORP. | HXW | 2025-12-11 |
| 00840493413907 | RIVA Posterior Fixation System | XENIX MEDICAL LLC | HXW | 2025-12-02 |
| 00840493413914 | RIVA Posterior Fixation System | XENIX MEDICAL LLC | HXW | 2025-12-02 |
| 00840493413921 | RIVA Posterior Fixation System | XENIX MEDICAL LLC | HXW | 2025-12-02 |
| 00840493413938 | RIVA Posterior Fixation System | XENIX MEDICAL LLC | HXW | 2025-12-02 |
| 00840493413945 | RIVA Posterior Fixation System | XENIX MEDICAL LLC | HXW | 2025-12-02 |
| 00199150044375 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | HXW | 2025-11-24 |
| 00199150044382 | Medtronic Reusable Instruments | MEDTRONIC SOFAMOR DANEK, INC. | HXW | 2025-11-24 |
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| 03662663153386 | Lineum Occipito-Cervico-Thoracic (OCT) Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663153393 | Lineum Occipito-Cervico-Thoracic (OCT) Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663153409 | Lineum Occipito-Cervico-Thoracic (OCT) Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663191784 | Polaris 5.5 Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663214872 | Vital Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663214889 | Vital Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663214896 | Vital Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-17 |
| 03662663146227 | Gallery Laminoplasty Fixation System | Highridge Medical, LLC | HXW | 2025-11-15 |
| 03662663113410 | Virage OCT Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-14 |
| 03662663131995 | Polaris 5.5 Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-14 |
| 03662663132008 | Polaris 5.5 Spinal Fixation System | Highridge Medical, LLC | HXW | 2025-11-14 |
| 03662663136785 | Polaris 4.75 Deformity System | Highridge Medical, LLC | HXW | 2025-11-14 |
| 03662663136792 | Polaris 4.75 Deformity System | Highridge Medical, LLC | HXW | 2025-11-14 |
| 03662663136808 | Polaris 4.75 Deformity System | Highridge Medical, LLC | HXW | 2025-11-14 |