Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list IDS Ltd with 6 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Dec 21, 2023: PICOSECOND Nd:YAG Laser 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.
| Dec 21, 2023 | PICOSECOND Nd:YAG Laser SystemK233018 · GEX | 510(k) clearances |
| Mar 29, 2023 | SMARTRION COMBI/Alexandrite & Long Pulsed Nd:YAG LaserK222485 · GEX | 510(k) clearances |
| Oct 5, 2018 | SHINY RPL SystemK181868 · ONF | 510(k) clearances |
| Feb 2, 2018 | SMAXEL CO2 Surgical Laser SystemK180036 · ONG | 510(k) clearances |
| Aug 1, 2017 | Q-Switched Nd:YAG Laser SystemK171079 · GEX | 510(k) clearances |
| Nov 7, 2012 | 25-Hydroxy Vitamin D EIA, Catalog #AC-57F1. Product Usage: The IDS 25-Hydroxy Vitamin D EIA kit is an enzymeimmunoassay intended for theClass II · Immunodiagnostic Systems is recalling the 25-Hydroxy Vitamin D EIA, AC-57F1 because the QC report was found to have an e | Device recalls |
| Sep 7, 1994 | OCTEIA INTACT PTHK941878 · CEW | 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
