Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Riverpoint Medical · Predicate Candidate Screening

27 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

30 daysmedian FDA review time
140 days90th percentile
27clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K253024ProZip Knotless ImplantRiverpoint Medical2025-10-16270
K252201HS FiberRiverpoint Medical2025-08-13300
K252144Iconix Speed Anchor; Iconix Speed HA+ AnchorRiverpoint Medical2025-07-30220
K243323Iconix Knotless AnchorRiverpoint Medical2024-11-19270
K243203OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft AnchorRiverpoint Medical2024-10-29280
K241282RibFix Titan™ Fixation SystemRiverpoint Medical2024-08-191040
K241577Iconix® AnchorRiverpoint Medical2024-07-03300
K240719OC JuggerKnot Soft AnchorRiverpoint Medical2024-04-11270
K240213Iconix Knotless AnchorRiverpoint Medical2024-02-23290
K240194ProCinch, QuadCinchRiverpoint Medical2024-02-21280
K231163HS Fiber SuturesRiverpoint Medical2024-01-052560
K233552IDEAL ZiploopRiverpoint Medical2023-11-30270
K233468Iconix AnchorRiverpoint Medical2023-11-14210
K203740JuggerKnot Soft AnchorRiverpoint Medical2021-02-12520
K202399OrthoButton FLRiverpoint Medical2020-09-18280
K190817HS FiberRiverpoint Medical2019-05-01300
K171060OrthoButton ALRiverpoint Medical2017-06-02530
K160655OrthoButton CLRiverpoint Medical2016-06-03870
K153307HS SutureTapeRiverpoint Medical2016-02-12880
K152795RiverLon (Nylon) SutureRiverpoint Medical2015-10-28300
K150288PDO Absorbable Punctum PlugRiverpoint Medical2015-08-282040
K140415MONOTEXRiverpoint Medical2014-03-26360
K120556VILET VILET QUICKRiverpoint Medical2012-05-23890
K103449BRACHYTHERAPY NEEDLES, RP SLEEVE, RP BRACHY-SPACER, GOLD MAKRiverpoint Medical2011-02-25940
K100461PDM, VILET, VILET QUICK, MONO Q, PLAIN GUT:# 6 CHROMIC GUTRiverpoint Medical2010-07-081401
K100006HS FIBER (POLYBLEND), RIVER BOND, RIVERSILK (SILK), RIVERPRORiverpoint Medical2010-05-101260
K092059RP CUTTING NEEDLERiverpoint Medical2009-09-24790

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda