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FDA Import Refusal AEK-2176174-6/10002/1 — Prollenium Medical Technologies Inc.

Prollenium Medical Technologies Inc. — FEI 3004423487

The FDA refused shipment AEK-2176174-6/10002/1 from Prollenium Medical Technologies Inc. (Canada) on Oct 23, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 23, 2026
Country
Canada
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
508

Recent inspections

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.