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 Paladin Medical with 14 510(k) clearances. The most recent is a 510(k) clearance dated Nov 3, 1999: NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYP….
| Nov 3, 1999 | NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)K993306 · HAM | 510(k) clearances |
| Aug 29, 1997 | MPC (MODEL 7000) EXTERNAL TEMPORARY PACEMAKER SYSTEMK970347 · DTE | 510(k) clearances |
| Jun 20, 1997 | STRATASYS FDM MEDMODELER SYSTEMK971290 · LLZ | 510(k) clearances |
| Dec 20, 1996 | ACU-CLENS CLEANING SYSTEM FOR CONTACT LENS CLEANINGK964222 · LYL | 510(k) clearances |
| Jun 29, 1995 | ENDO-BEND(TM) SHAVERK950054 · HRX | 510(k) clearances |
| Nov 29, 1993 | CORE PREVENT MATTRESS MODIFICATIONK935220 · FMW | 510(k) clearances |
| May 21, 1993 | SHARPE ENDOSPONGE ASPIIRATORK921015 · HET | 510(k) clearances |
| May 20, 1993 | SHARPE ENDOTENACULUMK915743 · HET | 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
