FDA applicant

Cell Ent., Inc.

Derwood, MD1 decision1989–19890 recalls

FDA records 1 decision for Cell Ent., Inc. (Derwood, MD) in 1989: 1 510(k) clearance. All are in product code KIT (Media And Components, Synthetic Cell And…). 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, hematology panel, where it files most

How often FDA has decided Cell Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cell Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cell Ent., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Cell”

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

Cell Robotics, Inc. 9 Cell Analysis, Inc. 1 Cell Constructs I, LLC 1 Cell Gen Therapeutics, LLC 1 Cell Bio-Systems, Inc. 1 Cell Culture Laboratories 1 Cell Store (Beijing) Biotechnology CO., LTD. 1

Cell Ent., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cell”