Infinity-Lock 3 102-1100
Infinity-Lock 3 102-1100 is a Class II device made by Xiros Ltd, cleared under FDA 510(k) K171680 on 30 Jun 2017 and listed in FDA GUDID since 4 Jun 2020 (UDI-DI 05060267131928), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05060267131928 | Date4 Jun 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK171680 | Date30 Jun 2017 | StatusActive |
Official records
- AccessGUDID record 05060267131928
- FDA 510(k) database K171680
Across registries
- FDA 510(k) K171680 decided 30 Jun 2017 Active
- FDA GUDID UDI-DI 05060267131928 listed 4 Jun 2020 Listed
Timeline
- Cleared FDA 510(k) K171680
- Listed FDA GUDID 05060267131928
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Infinity-Lock 3
- Generic name
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Model / Ref / Catalog
- 102-1100
- Primary DI / UDI-DI
- 05060267131928
- 510(k) Number
- FDA product code
- GAT
- GMDN term
- Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
- Device class
- Class II
- Regulation number
- 878.5000
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
Similar devices in this category
Other devices filed under Polyester suture, non-bioabsorbable, multifilament.
- Graft Fixation System 20049 by PARCUS MEDICAL LLC
- Graft Fixation System 20056S by PARCUS MEDICAL LLC
- FSSB A017PEG by Surgical Specialties México, S. de R.L. de C.V.
- FUMEDICA H26-2723N by Surgical Specialties México, S. de R.L. de C.V.
- FortiTex Suture, USP #2, blue, needle 100.356 by 41medical AG
- TEVDEK IPN928577 LSI-100009 by TELEFLEX INCORPORATED