FirmLabelled 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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Stanley Black & Decker and its 2 subsidiaries with 11 510(k) clearances and 10 device recalls. The most recent is a device recall dated Nov 21, 2019: The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Stanley Black & Decker and its 2 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 21, 2019 | The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax FMHT77506. These producClass II · The products are labeled as Class II lasers. However, the level of laser radiation emitted by the distributed products m | Device recalls |
| Mar 2, 1982 | CAST CUTTER/CAST SAW/INSTRUMENTK820351 · LGH | 510(k) clearances |
| Nov 2, 1981 | 150 DRIVER REAMERK812437 · GEY | 510(k) clearances |
| Nov 2, 1981 | 450/800 DRILLK812436 · HBC | 510(k) clearances |
| Nov 2, 1981 | DUAL MPC CHARGERK812439 · | 510(k) clearances |
| Nov 2, 1981 | POWER PACKK812440 · | 510(k) clearances |
| Nov 2, 1981 | SAGITTAL SAWK812438 · GEY | 510(k) clearances |
| Mar 19, 1980 | POWER PACKK800314 · KIJ | 510(k) clearances |
| Mar 19, 1980 | DUAL MPC CHARGERK800315 · KIJ | 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
