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 TRUMPF and its 3 subsidiaries with 31 device recalls and 4 510(k) clearances. The most recent is a device recall dated Jul 24, 2013: ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to ….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, TRUMPF and its 3 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 24, 2013 | ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.Class III · An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column. | Device recalls |
| Oct 26, 2010 | TRULIGHT 5520 AND TRULIGHT 5320K102758 · FSY | 510(k) clearances |
| Sep 28, 2009 | ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)K091246 · FSS | 510(k) clearances |
| Jun 22, 2006 | ILEDK061317 · FSY | 510(k) clearances |
| Jun 13, 2001 | TRUMPF SURGICAL LIGHTS, MODELS 301,501,701,1001K011693 · FSY | 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
