LineSider ASY-01110
LineSider ASY-01110 is a Class II device made by Integrity Implants Inc., listed in FDA GUDID since 4 Mar 2024 (UDI-DI 00840200409537), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00840200409537 | Date4 Mar 2024 | StatusListed |
Official records
- AccessGUDID record 00840200409537
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LineSider
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Model / Ref / Catalog
- ASY-01110
- Primary DI / UDI-DI
- 00840200409537
- FDA product code
- KWP, NKB
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class II
- Regulation number
- 888.3050, 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Orthopaedic inorganic implant inserter/extractor, reusable.
- 702624 by Stryker GmbH
- Unity Total Knee System 1230124 by CORIN LTD
- AXSOS 370003 by Stryker GmbH
- APEX Knee System WS-30051 by OMNIlife science, Inc.
- Femoral Prosthesis 31-473601 by Biomet Orthopedics, Inc.
- Trauma Fixation Systems 14-441051 by Biomet Orthopedics, Inc.
- LPS 2987-72-035 298772035 by DEPUY (IRELAND)
- CONDUIT LET30200T by MEDOS INTERNATIONAL SARL
- Identity™ SBRV9301 by Zimmer, Inc.
- TriFit TS Blade Stem 695.501 by CORIN LTD