FDA applicant

Mission Pharmacal Comp

New York, NY1 decision1998–19980 recalls

FDA records 1 decision for Mission Pharmacal Comp (New York, NY) in 1998: 1 510(k) clearance. All are in product code LKY (Device, External Penile Rigidity). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Mission Pharmacal Comp’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mission Pharmacal Comp since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mission Pharmacal Comp’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 “Mission”

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

Mission Pharmacal Co. 3 Mission White Dental, Inc. 2 Mission Diagnostics 2 Mission Dental, Inc. 2 Mission Medicl Devices 1

Mission Pharmacal Comp

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mission”