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 Axelgaard Manufacturing with 11 510(k) clearances. The most recent is a 510(k) clearance dated Feb 13, 2014: PALS PLATINUM NEUROSTIMULATION ELECTRODES.
| Feb 13, 2014 | PALS PLATINUM NEUROSTIMULATION ELECTRODESK132422 · GXY | 510(k) clearances |
| Jul 17, 2013 | VALUTRODE NEUROSTIMLATION ELECTRODESK130987 · GXY | 510(k) clearances |
| Jun 18, 2008 | COMFORT IONTOPHORESIS ELECTRODES/ BUFFERED IONTOPHORESIS ELECTRODE TREATMENT, MODEL SMALL DDS275, MEDIUM DDM325, LARGE DK080580 · EGJ | 510(k) clearances |
| Aug 22, 2002 | ULTRASTIM KITK013532 · GZJ | 510(k) clearances |
| Jun 16, 2000 | ULTRASTIM ELECTRODE, MODEL US4040K000947 · GXY | 510(k) clearances |
| Apr 13, 2000 | PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200K000206 · DRX | 510(k) clearances |
| Dec 18, 1998 | EVERLAST NEUROSTIMULATION ELECTRODES 2X 2,MODEL # EL2020K983741 · GXY | 510(k) clearances |
| May 9, 1997 | VALUETRODEK970426 · GXY | 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
