510(k) Report

FDA applicant

Pilgrim Plastic Products Co.

Boston, MA1 decision1984–19840 recalls

FDA records 1 decision for Pilgrim Plastic Products Co. (Boston, MA) in 1984: 1 510(k) clearance. All are in product code HCC (Device, Biofeedback). 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, neurology panel, where it files most

How often FDA has decided Pilgrim Plastic Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pilgrim Plastic Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pilgrim Plastic Products Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Pilgrim Plastic Products Co.’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 “Pilgrim”

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