Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Research Instruments Ltd and its 1 subsidiaries with 9 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jan 23, 2017: EZ-Tip Singles, EZ-Tip Vial of 20, EZ-Grip.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Research Instruments Ltd and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jan 23, 2017 | EZ-Tip Singles, EZ-Tip Vial of 20, EZ-GripK161275 · MQH | 510(k) clearances |
| Jul 18, 2016 | RI Witness Embryology Heated PlateK160504 · MQG | 510(k) clearances |
| Mar 11, 2016 | Integra 3; Model Numbers: 6-54-100, 6-54-110, 6-54-150, 6-54-160 Product Usage: The Rl TDU500 Micromanipulator for Assisted ReproductionClass II · The units have been fitted with a potentially faulty power supply cable. | Device recalls |
| Feb 18, 2015 | SATURN 5 LASERK141434 · MRX | 510(k) clearances |
| May 16, 2014 | BIOPSY PIPETTESK133257 · MQH | 510(k) clearances |
| Jul 13, 2012 | RI MSC (MIGRATION SEDIMENTATION CHAMBER)K112413 · MQK | 510(k) clearances |
| Aug 25, 2009 | SATURN ACTIVE LASER SYSTEMK083208 · MRX | 510(k) clearances |
| Mar 12, 2007 | SATURN 3 LASER SYSTEMK060764 · MRX | 510(k) clearances |
| Nov 22, 2000 | MICROMANIPULATORK003142 · MQJ | 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
