Medical device makerLabelled 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 13, 2026, FDA's public records list Gi Supply with 10 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Apr 19, 2023: Renova RP Centesis Pump.
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.
| Date | Record | Source |
|---|---|---|
| Apr 19, 2023 | Renova RP Centesis PumpK221042 · BTA | 510(k) clearances |
| Sep 30, 2020 | EverLift Submucosal Lifting AgentK202376 · PLL | 510(k) clearances |
| Jun 20, 2020 | EverLift Submucosal Lifting AgentK191923 · PLL | 510(k) clearances |
| Jan 28, 2016 | Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most components. Packed sterilClass II · Customers have reported that the pinch clamp on the RP Bag was missing. Ascetic fluid from the abdominal cavity may spla | Device recalls |
| Sep 24, 2003 | GI SUPPLY BILIARY STENTK031360 · FGE | 510(k) clearances |
| Sep 25, 2001 | HP-ONEK012411 · LYR | 510(k) clearances |
| Feb 14, 1997 | RUNYON LARGE VOLUME PARACENTESIS KITK970187 · LRO | 510(k) clearances |
| Feb 14, 1997 | GI SUPPLY PARACENTESIS PUMPK970186 · BTA | 510(k) clearances |
| Apr 20, 1995 | HP-FASTK944903 · LYR | 510(k) clearances |
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
