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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Microline Pentax with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jan 8, 2002: MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS, MODEL….
| Date | Record | Source |
|---|---|---|
| Jan 8, 2002 | MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS, MODEL M/L-10K013695 · GCJ | 510(k) clearances |
| Oct 21, 1998 | ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTSK982984 · GEI | 510(k) clearances |
| May 29, 1998 | DISPOSABLE RE-NEW FORCEPSK981389 · GEI | 510(k) clearances |
| May 20, 1998 | ELECTROSURGICAL CAUTERY PROBESK981188 · GEI | 510(k) clearances |
| Mar 27, 1998 | 3 MM SELEC-TIP LAPAROSCOPIC SCISSORSK980758 · GEI | 510(k) clearances |
| Jan 22, 1998 | RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPSK974066 · GEI | 510(k) clearances |
| Mar 28, 1997 | SELECTA-TIP LAPAROSCOPIC SCISSORSK970826 · GEI | 510(k) clearances |
| Aug 9, 1996 | RE-NEW LAPAROSCOPIC INSTRUMENTSK962119 · GEI | 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
