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 Endocare, Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated Jun 14, 2010: CRYOCARE CS SURGICAL SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jun 14, 2010 | CRYOCARE CS SURGICAL SYSTEMK101333 · GEH | 510(k) clearances |
| Aug 28, 2006 | CRYOCARE CN2 SYSTEMK062175 · GEH | 510(k) clearances |
| Feb 28, 2006 | CRYOCARE CS SURGICAL SYSTEMK060279 · GEH | 510(k) clearances |
| Feb 25, 2005 | MODIFICATION TO CRYOCARE CS SURGICAL SYSTEMK050347 · GEH | 510(k) clearances |
| Aug 12, 2003 | CRYOCARE CS SURGICAL SYSTEMK032333 · GEH | 510(k) clearances |
| Dec 5, 2002 | CRYOCARE SURGICAL SYSTEM, MODEL CRYO 20K023757 · GEH | 510(k) clearances |
| Jun 6, 2002 | MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSEK021010 · OCL | 510(k) clearances |
| Feb 5, 2002 | ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEMK020082 · LKY | 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
