Invictus 17053
Invictus 17053 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 17 Jun 2020 (UDI-DI 00190376204659), 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 | Number00190376204659 | Date17 Jun 2020 | StatusListed |
Official records
- AccessGUDID record 00190376204659
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Invictus
- Generic name
- Manual orthopaedic bender, reusable
- Model / reference
- 17053
- Primary DI / UDI-DI
- 00190376204659
- FDA product code
- HXW
- GMDN term
- Manual orthopaedic bender, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Manual orthopaedic bender, reusable.
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- ORTHOLOC 3Di 59250010 by WRIGHT MEDICAL TECHNOLOGY, INC.
- NA IP 8405-50 by aap Implantate AG
- A.L.P.S.1ST MTP FUSION PLATE BENDER 231220212 by Biomet Orthopedics, Inc.
- AXSOS 705006 by Stryker Corp.
- NA IP 2506-00 by aap Implantate AG
- 3.5 POST LATERAL / OLECRANON BENDER 2312-18-008 231218008 by Biomet Orthopedics, Inc.