Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 3 companies' records, each linked to the record.
As of Nov 14, 2026, FDA's public records list Halma and its 3 subsidiaries with 73 510(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, Halma and its 3 subsidiaries
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 31, 2015 | KEELER DISPOSABLE TONOMATE, KEELER DISPOSABLE TONOMATE, BOX OF 100K152644 · HKY | 510(k) clearances |
| Sep 10, 2015 | Keeler Slit LampK151394 · HJO | 510(k) clearances |
| Sep 17, 2014 | D-KAT Z-YPEK142179 · HKY | 510(k) clearances |
| Jul 11, 2014 | KEELER SLIT LAMP H-SERIES DIGITAL (HALOGEN BULB OPTION), KEELER SLIT LAMP H-SERIES DIGITAL (LED OPTION)K140451 · HJO | 510(k) clearances |
| Jun 17, 2014 | KEELER KAPTURE SOFTWAREK140450 · HKI | 510(k) clearances |
| Feb 21, 2014 | T-TYPE D-KAT, R-TYPE D-KATK133234 · HKY | 510(k) clearances |
| Dec 23, 2013 | CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBESK131787 · 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
