Iconix Knotless T
510(k) K262677
Iconix Knotless T is a Class II device made by Riverpoint Medical LLC, cleared under FDA 510(k) K262677 on 27 Aug 2026, 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 | FDA 510(k)SESE | NumberK262677 | Date27 Aug 2026 | StatusActive |
Official records
- FDA 510(k) database K262677
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MBI
- FDA applicant
- Riverpoint Medical
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3040
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue).
- JuggerKnot® 912064 by Biomet Orthopedics, Inc.
- Responsive Arthroscopy Stealth and Mini Stealth All-Suture Anchors by RESPONSIVE ARTHROSCOPY
- Meniscal Repair Device by Linvatec Corp.
- TOGGLELOC XL WITH ZIPLOOP INLINE 110005090 by Biomet Orthopedics, Inc.
- V-Lox Peek CF Suture Anchor 10254T by PARCUS MEDICAL LLC
- Arthrex® AR-5100-09 by Arthrex, Inc.
- INTRAFIX TIBIAL SHEATH by Depuy Mitek, A Johnson & Johnson Company
- Y-KNOT Y1802 by Conmed Corporation
- Grappler Interference Screw System by Paragon 28
- Aevumed PROTEKT Suture Anchor by Aevumed, Inc.