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 Ultracell Medical Technologies with 24 510(k) clearances. The most recent is a 510(k) clearance dated Aug 24, 2001: ULTRACELL ABSORBENT STICK.
| Aug 24, 2001 | ULTRACELL ABSORBENT STICKK012196 · HOZ | 510(k) clearances |
| Dec 17, 1997 | ULTRACELL SUCTION SPONGEK972634 · GDY | 510(k) clearances |
| Dec 17, 1997 | ULTRACELL SUCTION SPONGEK972633 · HOZ | 510(k) clearances |
| Dec 9, 1997 | ULTRACELL NEURO SPONGESK973083 · HBA | 510(k) clearances |
| Nov 24, 1997 | VISUAL ENDOSCOPIC NON-ALCOHOL ULTRACELL SPONGE (VENUS)K973558 · FEB | 510(k) clearances |
| Nov 18, 1997 | ULTRACELL PACKING WITH SLEEVEK973085 · EMX | 510(k) clearances |
| Oct 1, 1997 | ULTRACELL SUCTION SPONGEK972635 · GBX | 510(k) clearances |
| Apr 21, 1997 | ULTRACELL NEURO SPONGESK970328 · HBA | 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
