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 15, 2026, FDA's public records list Interlace Medical with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 2, 2011: SURGISURE TISSUE REMOVAL SYSTEM.
| Mar 2, 2011 | SURGISURE TISSUE REMOVAL SYSTEMK103741 · GCJ | 510(k) clearances |
| Oct 15, 2010 | MYOSURE ROD LENS SCOPE SEALSK102686 · HIH | 510(k) clearances |
| Mar 30, 2010 | MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEMK100559 · HIH | 510(k) clearances |
| Oct 23, 2009 | MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEMK091100 · HIH | 510(k) clearances |
| Aug 21, 2009 | MYOSURE ROD LENS HYSTEROSCOPEK091465 · HIH | 510(k) clearances |
| Jul 23, 2008 | INTERLACE MEDICAL OPERATIVE HYSTEROSCOPY SYSTEMK081070 · HIH | 510(k) clearances |
| Apr 17, 2008 | INTERLACE MEDICAL HYSTEROSCOPIC MORCELLATION SYSTEMK073690 · HIH | 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
