Smooth PEG
33 catalogue numbers from 131227013, listed by Biomet Orthopedics, United States, under Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite. 6 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (2), Zhejiang (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 53 |
| Suzhou Ahno Medical Devices Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 17 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 74 |
| Shanghai JPY ION-Tech Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 70 |
Record
| Listed by | Biomet Orthopedics, United States |
|---|---|
| FDA product code | LXT |
| Device type | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3030 |
| Record published | 2022-09-07 |
| Record revised | 2025-05-30 (version 7) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 131227013 | 2.2 mm x 13 mm | In distribution |
| 131227024 | 2.2 mm x 24 mm | In distribution |
| 131227026 | 2.2MM X 26MM | In distribution |
| 131227011 | 2.2MM X 11MM | In distribution |
| 131227013 | 2.2MM X 13MM | In distribution |
| 131227014 | 2.2MM X 14MM | In distribution |
| 131227012 | 2.2 mm x 12 mm | In distribution |
| 131227009 | 2.2MM X 9MM | In distribution |
| 131227015 | 2.2 mm x 15 mm | In distribution |
| 131227012 | 2.2MM X 12MM | In distribution |
| P28000 | 2.0 MM X 28 MM | In distribution |
| 131227020 | 2.2MM X 20MM | In distribution |
| 131227016 | 2.2MM X 16MM | In distribution |
| 131227016 | 2.2 mm x 16 mm | In distribution |
| 131227022 | 2.2 mm x 22 mm | In distribution |
| 131227030 | 2.2 mm x 30 mm | In distribution |
| 131227008 | 2.2MM X 8MM | In distribution |
| 131227018 | 2.2MM X 18MM | In distribution |
| 131227009 | 2.2 mm x 9 mm | In distribution |
| 131227010 | 2.2 mm x 10 mm | In distribution |
| 131227008 | 2.2 mm x 8 mm | In distribution |
| 131227024 | 2.2MM X 24MM | In distribution |
| 131227014 | 2.2 mm x 14 mm | In distribution |
| 131227026 | 2.2 mm x 26 mm | In distribution |
| 131227010 | 2.2MM X 10MM | In distribution |
| 131227022 | 2.2MM X 22MM | In distribution |
| 131227011 | 2.2 mm x 11 mm | In distribution |
| 131227020 | 2.2 mm x 20 mm | In distribution |
| 131227018 | 2.2 mm x 18 mm | In distribution |
| 131227028 | 2.2 mm x 28 mm | In distribution |
| 131227030 | 2.2MM X 30MM | In distribution |
| 131227028 | 2.2MM X 28MM | In distribution |
| 131227015 | 2.2MM X 15MM | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| True/LOK Monolateral/Bilateral Fixator | Orthofix SRL | 206 |
| Truelok System | Orthofix SRL | 138 |
| Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite | Synthes Gmbh | 60 |
| TrueLok Evo | Orthofix SRL | 60 |
| IJS | Skeletal Dynamics L.L.C. | 48 |
| Arbor | Globus Medical, Inc. | 46 |
| Multi-Directional Screw | Biomet Orthopedics | 44 |
| LCP | Synthes Gmbh | 40 |
| Lock Screw Square Drive | Biomet Orthopedics | 40 |
| A.l.p.s.® | Biomet Orthopedics | 32 |
| Cannulated Cancellous LAG Screw | Biomet Orthopedics | 31 |
| Smooth Locking PEG | Biomet Orthopedics | 28 |
Showing 12 of 261. All products under Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K020905 | 2002-04-15 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.