Medical device makerLabelled 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 14, 2026, FDA's public records list Indus Medicare Limited with 8 510(k) clearances and 2 warning letters. The most recent is a warning letter dated Feb 17, 2021: Warning letter: Medical Devices.
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 17, 2021 | Warning letter: Medical DevicesCDRH | Warning letters |
| May 4, 2020 | Warning letter: CAPA, MDR reporting, Design controlsCDRH | Warning letters |
| Apr 8, 2003 | INVIGRAK022614 · HIS | 510(k) clearances |
| Mar 4, 2002 | INVIGRAK020223 · HIS | 510(k) clearances |
| Mar 21, 2000 | INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVOREDK000040 · HIS | 510(k) clearances |
| Mar 21, 2000 | INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVOREDK000039 · HIS | 510(k) clearances |
| Mar 21, 2000 | INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVOREDK000038 · HIS | 510(k) clearances |
| Dec 29, 1999 | INVIGRAK993693 · HIS | 510(k) clearances |
| Aug 2, 1999 | INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)K992438 · LTZ | 510(k) clearances |
| Jun 15, 1999 | INVIGRAK991374 · HIS | 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
