Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Riverpoint Medical with 47 device recalls and 40 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 2026: Fast Absorbing PGLA.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 29, 2026 | Fast Absorbing PGLAK263073 · GAM | 510(k) clearances |
| Aug 27, 2026 | Iconix Knotless TK262677 · MBI | 510(k) clearances |
| Mar 11, 2026 | Strut Suture; No-Tie ButtonK253693 · MBI | 510(k) clearances |
| Feb 27, 2026 | LigaMendK253695 · MBI | 510(k) clearances |
| Oct 16, 2025 | ProZip Knotless ImplantK253024 · GAT | 510(k) clearances |
| Aug 13, 2025 | HS FiberK252201 · GAT | 510(k) clearances |
| Jul 30, 2025 | Iconix Speed Anchor; Iconix Speed HA+ AnchorK252144 · MBI | 510(k) clearances |
| Mar 20, 2025 | RootMend MRRK243988 · MBI | 510(k) clearances |
| Oct 25, 2023 | Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 39Class II · Use of a 1.4 drill in hard bone conditions caused increased insertion forces leading to subsequent failures of the inser | Device recalls |
| Dec 9, 2020 | Covidien CV-9590 Velosorb Fast Braided Fast absorbable Suture 14 Metric 36" 90 cm, GS-24 Taper 1/2 40 mm, undyed, UDI: 10884521151307Class II · Due to a manufacturing error, there is a potential that sutures may exhibit inadequate tensile strength. This could pot | Device recalls |
| Aug 3, 2020 | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30" KV-11, TaperCutting, Product Number: CV2293, UDI: 2088452115158Class II · The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, | Device recalls |
| Aug 3, 2020 | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-12 Cutting SV426, UDI: 20884521151731 - Product Usage: indicaClass II · The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, | Device recalls |
| Aug 3, 2020 | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" CV-25 Taper, Product Number: CV3100, UDI: 20884521150901 - ProdClass II · The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, | Device recalls |
| Aug 3, 2020 | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" GS-21 Taper CV946, UDI: 20884521151298 - Product Usage: indicatedClass II · The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, | Device recalls |
| Aug 3, 2020 | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" GS-25 CV604, UDI: 20884521152288 - Product Usage: indicated forClass II · The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, | Device recalls |
| Aug 3, 2020 | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" PC-11 SV487G, UDI: 10884521149595 - Product Usage: indicated Class II · The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built