SCREWDRIVER
- Primary DI
- 00888118081605
- Brand
- SCREWDRIVER
- Company
- KLS-Martin L.P.
- Model
- 51-512-90-07
- Published
- 2018-09-26
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HXX | SCREWDRIVER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HXX | Screwdriver | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118081605 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118081605 | 00888118081605 | 888118081605 | 0888118081605 |
GMDN Terms#
| Term | Definition |
|---|---|
| Implantable craniofacial bone distractor expansion tool, home-use | A hand-held, manual device intended to be used by a layperson to adjust an intraoral implantable craniofacial bone distractor to progressively lengthen the distractor, typically during expansion of the maxilla. It is used by the patient in the home for daily, gradual distraction. This is a single-patient 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
- Premarket exempt
- true
- Lot or batch
- true
- 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 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 07640221373076 | PERLA ® TL | SpineArt SA | HXX | 2026-05-07 |
| 09120125220259 | Shark Screw® driver acl | surgebright GmbH | HXX | 2026-04-30 |
| 08806373894213 | LOSPA/BENCOX | Corentec Co., Ltd | HXX | 2026-04-10 |
| 08806373899720 | LOSPA/BENCOX | Corentec Co., Ltd | HXX | 2026-04-10 |
| 08806373887789 | BENCOX Surgical Instruments | Corentec Co., Ltd | HXX | 2026-01-12 |
| 08806373892660 | BENCOX Surgical Instruments | Corentec Co., Ltd | HXX | 2026-01-12 |
| 07640332475294 | PERLA ® | SpineArt SA | HXX | 2025-11-10 |
| 07640332475300 | PERLA ® | SpineArt SA | HXX | 2025-11-10 |
| 07640332475317 | PERLA ® | SpineArt SA | HXX | 2025-11-10 |
| 08059386744253 | Orthopaedic Surgical Instruments | CITIEFFE SRL | HXX | 2025-11-06 |
| 08059386742266 | Orthopaedic Surgical Instruments | CITIEFFE SRL | HXX | 2025-11-05 |
| 09348215164737 | Turbine X Driver - Green | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215164744 | Turbine X Driver – Red | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215164751 | MI (Mini Incision) Driver - Red | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215164768 | MI (Mini Incision) Driver - Green | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215164775 | O (Turbine OP) Driver - Green | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165017 | 2.9 Knotted Driver | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165024 | Vector Knotted Driver | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165123 | 5.5 Knotless Driver | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165130 | Screw Driver | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165178 | Simple Driver (Black) | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165185 | Simple Driver (Orange) | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165208 | Tendonesis Chamfer Reamer | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| 09348215165284 | Staple Shaft | SIGNATURE ORTHOPAEDICS PTY LTD | HXX | 2025-10-10 |
| G791CDRASS200 | WishFIX | Red Star Contract Manufacturing Inc. | HXX | 2025-10-06 |
| G791SDRASS200 | WishFIX | Red Star Contract Manufacturing Inc. | HXX | 2025-10-06 |
| 09120125220037 | Shark Screw® coupling | surgebright GmbH | HXX | 2025-09-16 |
| 09120125220228 | Shark Screw® driver | surgebright GmbH | HXX | 2025-09-16 |
| 08800071006848 | Surgical Instrument | OSTEONIC CO.,Ltd. | HXX | 2025-06-24 |
| 08800071024248 | Signex | OSTEONIC CO.,Ltd. | HXX | 2025-06-24 |