Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list HGM Inc. with 23 510(k) clearances. The most recent is a 510(k) clearance dated Aug 11, 1995: SMART PLUG.
| Date | Record | Source |
|---|---|---|
| Aug 11, 1995 | SMART PLUGK950120 · GEX | 510(k) clearances |
| Nov 10, 1994 | HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBEK931072 · HJM | 510(k) clearances |
| Mar 1, 1994 | HGM ILLUMINATING IMAGING ENDOCULAR PROBEK931784 · HQF | 510(k) clearances |
| Sep 23, 1993 | HGM SCANMAN PLUSK933333 · GEX | 510(k) clearances |
| Aug 19, 1993 | Q-11 OPHTHALMIC LASERK931499 · GEX | 510(k) clearances |
| Aug 17, 1993 | HGM ASPIRATING ENDOOCULAR(TM) PROBEK925663 · HQF | 510(k) clearances |
| Jun 22, 1993 | E-25 KRYPTON ION LASER (SURGICA K5)K930543 · GEX | 510(k) clearances |
| May 3, 1988 | MODEL PC ARGON LASERK880908 · GEX | 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
