Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of HalmaLabelled 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 14, 2026, FDA's public records list Keeler Instruments with 60 510(k) clearances. The most recent is a 510(k) clearance dated Feb 8, 2019: Keeler TonoCare Tonometer.
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 8, 2019 | Keeler TonoCare TonometerK181143 · HKX | 510(k) clearances |
| Dec 8, 2011 | CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTERK112093 · HRN | 510(k) clearances |
| Dec 10, 2010 | PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417-P-2000K093298 · HKX | 510(k) clearances |
| Mar 9, 2010 | PSL CLASSIC SLIT LAMPK100500 · HJO | 510(k) clearances |
| Nov 6, 2006 | CRYOMATICK062412 · HRN | 510(k) clearances |
| May 23, 2006 | VANTAGE INDIRECT OPHTHALMOSCOPEK060822 · HLI | 510(k) clearances |
| Nov 26, 2003 | KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004K032087 · HLJ | 510(k) clearances |
| Dec 21, 1999 | KEELER CRYO MASTER & PROBESK992954 · HRN | 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
