Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of EnovisLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Trilliant Surgical with 23 device recalls and 18 510(k) clearances. The most recent is a 510(k) clearance dated Feb 23, 2022: Arsenal Ankle Plating System.
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.
| Feb 23, 2022 | Arsenal Ankle Plating SystemK212378 · HRS | 510(k) clearances |
| Aug 12, 2019 | Arsenal Plating SystemK191009 · HRS | 510(k) clearances |
| Oct 26, 2018 | Two-Step Implant SystemK181898 · HWC | 510(k) clearances |
| Mar 27, 2018 | Ratcheting Cannulated Driver Handle, Catalog #: 210-00-004, Rx Only, Non SterileClass II · Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation o | Device recalls |
| Mar 27, 2018 | Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non SterileClass II · Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation o | Device recalls |
| Dec 11, 2017 | SNIPER STAPLE SYSTEM, NON-STERILEK172405 · JDR | 510(k) clearances |
| Nov 16, 2017 | Minimally Invasive Bunion Plating SystemK172178 · HRS | 510(k) clearances |
| Apr 20, 2017 | Sniper Staple SystemK162354 · JDR | 510(k) clearances |
| Dec 8, 2016 | Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O The product is a component of a system indicated for the fixatiClass II · Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to the field with a printing error where k-wir | Device recalls |
| Sep 2, 2016 | Model 208-70-110, Long Thread Tiger Large Cannulated Headless Screw, 7 x 110 mm labeled as "7.0 x 110mm LTTHCS REF 208-70-110 QTY 30 LOTClass II · Screws were identified as having the incorrect part number and lot number marked upon them. The part number incorrectly | Device recalls |
| Apr 22, 2016 | Gridlock Ankle Plating SystemK160177 · HRS | 510(k) clearances |
| Jan 14, 2016 | Tiger Cannulated Screw SystemK153338 · HWC | 510(k) clearances |
| Aug 6, 2015 | 7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula Plate, Part # 300-60-002 NON-STERIClass II · The affected parts subject to the recall are out of specification, resulting in in the loss of the optimal locking screw | Device recalls |
| Jul 31, 2015 | 2.4, 3.0, and 4.0 mm Gridlock Screw Driver Bit, Model Number 310-30-003, Lot Number TSL002605, NON-STERILE. For use with the Gridlock PlatiClass II · Gridlock screw driver bits for the Gridlock Plating System were identified to be out of specification and have the poten | Device recalls |
| Jul 20, 2015 | Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, 20 mm; Concave Reamer Head 22 mm; Convex Reamer Head, 16 mm; CoClass II · The cannulation of the Concave and Convex Reamer Heads may be too small to allow the Guide Pin to freely pass through. | Device recalls |
| Jul 20, 2015 | Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE; Combined Tiger/Headless Screw Part # 210-99-101 NON-STERILE; These are componentsClass II · Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Systems were reported to occasionally be diffi | 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
