Medical device makerLabelled 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 14, 2026, FDA's public records list Clearmedical, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 11, 2005: REPROCESSED MULTIPLE CLIP APPLIERS.
| Jul 11, 2005 | REPROCESSED MULTIPLE CLIP APPLIERSK033579 · NMJ | 510(k) clearances |
| Jul 11, 2005 | REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERSK033578 · NLL | 510(k) clearances |
| Jun 3, 2005 | REPROCESSED TROCARSK033591 · KBG | 510(k) clearances |
| Jul 27, 2004 | REPROCESSED SURGICAL SCISSORS AND GRASPERSK033592 · GEI | 510(k) clearances |
| Nov 20, 2003 | REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPSK033593 · NLU | 510(k) clearances |
| Jul 15, 2003 | CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFFK031416 · DXQ | 510(k) clearances |
| Jul 3, 2002 | CLEARMEDICAL/NELLCOR OXISENSOR II, ADULT, MODEL D-25/D-25LK012600 · NLF | 510(k) clearances |
| Jul 3, 2002 | CLEARMEDICAL/NELLCOR OXISENSOR II, NEONATAL/ADULT, MODEL N-25K012609 · NLF | 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
