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 14, 2026, FDA's public records list GK Photonics with 6 device recalls. The most recent is a device recall dated Jul 10, 2019: Burstberry Laser Projection Series.
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.
| Jul 10, 2019 | Burstberry Laser Projection SeriesClass II · The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual | Device recalls |
| Jul 10, 2019 | Logolas Laser Projection SeriesClass II · The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual | Device recalls |
| Jul 10, 2019 | Maxim Laser Projection SeriesClass II · The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual | Device recalls |
| Jul 10, 2019 | Atom Laser Projection SeriesClass II · The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual | Device recalls |
| Jul 10, 2019 | ClubMax Laser Projection SeriesClass II · The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual | Device recalls |
| Jul 10, 2019 | Spectrum Laser Projection SeriesClass II · The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual | Device recalls |
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
