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.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Mectra Laboratories, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jun 29, 2012: TUBALGATOR.
| Jun 29, 2012 | TUBALGATORK113080 · HIN | 510(k) clearances |
| Mar 10, 2004 | ELECTRO-LUBEK033880 · GEI | 510(k) clearances |
| Nov 8, 2002 | PNEUMOPERITONEUM INSUFFLATION NEEDLEK021247 · HIF | 510(k) clearances |
| Mar 3, 2000 | ENDOSCOPIC ANTI FOG DEVICEK993604 · OCT | 510(k) clearances |
| Apr 5, 1996 | SUCTION CAUTERY PROBEK955352 · GEI | 510(k) clearances |
| Feb 18, 1994 | MECTRA TROCARK934547 · GCJ | 510(k) clearances |
| Feb 15, 1994 | GRASPERSK935382 · GCJ | 510(k) clearances |
| Sep 23, 1993 | INSUFFLATION TUBINGK925691 · HIF | 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
