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 15, 2026, FDA's public records list Life-Tech International with 68 510(k) clearances. The most recent is a 510(k) clearance dated Jul 6, 2000: PROLONG, MODELS PL50, PL100, PL150.
| Jul 6, 2000 | PROLONG, MODELS PL50, PL100, PL150K001129 · CAZ | 510(k) clearances |
| Dec 10, 1996 | MAXISTIMK955031 · KOI | 510(k) clearances |
| Dec 10, 1996 | EZ STIMK954505 · KOI | 510(k) clearances |
| Nov 30, 1995 | PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954315 · FEN | 510(k) clearances |
| Oct 17, 1995 | URODYNAMICS TUBING AND INFUSION SETSK954341 · FEN | 510(k) clearances |
| Oct 5, 1995 | UROPUMP TUBE & DAMPING CHAMGERK953451 · FEN | 510(k) clearances |
| Sep 8, 1995 | UROVISION JANUSK953353 · FEN | 510(k) clearances |
| Jun 13, 1995 | EAR-A-GATORK946108 · KHH | 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
