Aria 48755701
Aria 48755701 is a Class I device made by Stryker Corp., listed in FDA GUDID since 14 Oct 2019 (UDI-DI 07613327006070), 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 | Number07613327006070 | Date14 Oct 2019 | StatusListed |
Official records
- AccessGUDID record 07613327006070
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aria
- Generic name
- Torque manipulation device
- Model / Ref / Catalog
- 48755701
- Primary DI / UDI-DI
- 07613327006070
- FDA product code
- LXH
- GMDN term
- Torque manipulation device
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT).
- Maxim® Instrumentation 32-347911 by Biomet Orthopedics, Inc.
- Knee Instruments 02.12.10.1230 by Medacta International SA
- Hip Instruments 01.26.10.0311 by Medacta International SA
- 2351-0050 by Stryker GmbH
- ACUMED HR-3101 by ACUMED LLC
- 28163CM by Karl Storz SE & CO. KG
- APEX Knee System WS-30051 by OMNIlife science, Inc.
- 0193-3800 by Stryker GmbH
- MENISCAL SUTURING SYSTEM by Dyonics, Inc.
- RADIAL OSTEOTOME MEDIAL BLADE 127x12 WITH SLOT 01.10.10.2067 by HPF SRL