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 StrykerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Stryker Communications with 20 device recalls and 4 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 2013: VISUM BLADE LED SURGICAL LIGHTING SYSTEM.
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.
| Dec 30, 2013 | VISUM BLADE LED SURGICAL LIGHTING SYSTEMK132747 · FSY | 510(k) clearances |
| Sep 25, 2012 | (l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat Panel and Navigation Arm The Spring Arm Circlip is partClass II · Stryker has become aware that there is a low likelihood of incomplete engagement of the Spring Arm Circlip during servic | Device recalls |
| May 6, 2010 | STRYKER SWITCHPOINT INFINITY 3 CONTROL SYSTEM, MODEL: 067-8001-000K100852 · OCS | 510(k) clearances |
| Apr 7, 2006 | VISUM LED SURGICAL LIGHTING SYSTEMK060802 · FSY | 510(k) clearances |
| Sep 2, 2004 | STRYKER SWITCHPOINT INFINITYK033132 · GCJ | 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
