Home › Device types › IDW
Dispensers, Paraffin
FDA product code IDW · Class 1 · Pathology
48
Registered devices
4
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
HistoPro® — RUSHABH INSTRUMENTS, LLCEpredia — SHANDON DIAGNOSTICS LIMITEDThermo Fisher — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDThermo Fisher — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDHistoPro® — RUSHABH INSTRUMENTS, LLCTissue-Tek® TEC™ 6 — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDHistoPro® — RUSHABH INSTRUMENTS, LLCEpredia — SHANDON DIAGNOSTICS LIMITEDTissue-Tek® TEC™ 6 — SAKURA FINETEK U.S.A., INC.Thermo Fisher — SHANDON DIAGNOSTICS LIMITEDThermo Fisher — SHANDON DIAGNOSTICS LIMITEDThermo Fisher — SHANDON DIAGNOSTICS LIMITEDTissue-Tek® TEC™ 6 — SAKURA FINETEK U.S.A., INC.Tissue-Tek® TEC™ 6 — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDTissue-Tek AutoTEC® a120 — SAKURA FINETEK U.S.A., INC.Tissue-Tek® TEC™ 6 — SAKURA FINETEK U.S.A., INC.HistoPro® — RUSHABH INSTRUMENTS, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-05-10 | LEICA BIOSYSTEMS NUSSLOCH GMBH | An issue with safe usage of the device was identified whereby toxic smoke and internal fire developed resulting from a problem associated with the sealing of th |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.