FDA applicant

Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger

New York, NY1 decision1989–19890 recalls

FDA records 1 decision for Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger (New York, NY) in 1989: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hemo-Sanitas, Inc. C/O Greenberg Irwin…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Hemo-Sanitas”

FDA records each applicant name separately; these may or may not be the same firm.

Hemo Sapiens, Inc. 2 Hemo-Barrier Technologies, Inc. 1

Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hemo-Sanitas”