LEVEL ONE ORTHOANCHOR
- Primary DI
- 00888118101839
- Brand
- LEVEL ONE ORTHOANCHOR
- Company
- KLS-Martin L.P.
- Model
- 50-345-15-91
- Published
- 2016-09-20
- 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
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | Dental | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118101839 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118101839 | 00888118101839 | 888118101839 | 0888118101839 |
GMDN Terms#
| Term | Definition |
|---|---|
| Craniofacial bone screw, non-bioabsorbable, sterile | A small, sterile, threaded rod with a slotted head intended to be implanted or inserted short-term in craniofacial bone (including the maxilla and/or mandible) for fracture fixation by direct interfragmentary stabilization of bone or by screwing plates in place; it may also be intended for transplanted bone fixation. It may be self-drilling/self-tapping and is made of a material that is not chemically degraded or absorbed via natural body processes [e.g., implant grade metal such as titanium (Ti)]. Its uses include repair of orbital fractures and fractures around the cranial sinuses, paediatric reconstructive surgery, craniotomy flap fixation, bone augmentation procedures. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(904)641-7746 | webcontact@klsmartin.com |
Regulatory Flags#
- DUNS number
- 826499238
- 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
- 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 |
|---|---|---|---|---|
| 00888118108357 | DISTRACTION, INTERNAL, STERILE | 51-556-20-81 | 2018-09-26 | |
| 00888118108364 | DISTRACTION, INTERNAL, STERILE | 51-557-20-81 | 2018-09-26 | |
| 00888118147226 | LEVEL ONE EXTREMITY | 26-950-64-04 | 2026-07-21 | |
| 00888118147233 | LEVEL ONE EXTREMITY | 26-950-65-04 | 2026-07-21 | |
| 00888118147240 | LEVEL ONE EXTREMITY | 26-950-66-04 | 2026-07-21 | |
| 00888118147257 | LEVEL ONE EXTREMITY | 26-950-67-04 | 2026-07-21 | |
| 00888118147264 | LEVEL ONE EXTREMITY | 26-950-68-04 | 2026-07-21 | |
| 00888118147271 | LEVEL ONE EXTREMITY | 26-950-69-04 | 2026-07-21 | |
| 00888118147714 | LEVEL ONE EXTREMITY | 26-950-58-04 | 2026-07-21 | |
| 00888118147721 | LEVEL ONE EXTREMITY | 26-950-59-04 | 2026-07-21 | |
| 00888118147738 | LEVEL ONE EXTREMITY | 26-950-62-04 | 2026-07-21 | |
| 00888118147745 | LEVEL ONE EXTREMITY | 26-950-63-04 | 2026-07-21 | |
| 00888118154620 | LEVEL ONE CMF | 25-315-92-91 | 2026-07-21 | |
| 00888118154637 | LEVEL ONE CMF | 50-743-06-09 | 2026-07-21 | |
| 00888118154644 | LEVEL ONE, STERILE | 25-433-97-71 | 2026-07-21 | |
| 00888118154651 | LEVEL ONE, STERILE | 25-438-97-71 | 2026-07-21 | |
| 00888118154668 | LEVEL ONE, STERILE | 25-439-91-71 | 2026-07-21 | |
| 00888118154675 | LEVEL ONE, STERILE | 25-486-97-71 | 2026-07-21 | |
| 00888118154682 | LEVEL ONE, STERILE | 25-487-97-71 | 2026-07-21 | |
| 00888118154699 | LEVEL ONE, STERILE | 50-817-15-71 | 2026-07-21 |
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| 07392532049644 | Astra Tech Implant System® | Dentsply Implants Manufacturing GmbH | DZE | 2025-11-04 |
| 07392532049651 | Astra Tech Implant System® | Dentsply Implants Manufacturing GmbH | DZE | 2025-11-04 |
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