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PlastiBell Circumcision Device

ASPEN SURGICAL PRODUCTS, INC. · Model 9217 · UDI-DI 00840113231607

FHG Prescription
2
510(k) clearances
42
Adverse events
0
Recalls
3
Facilities

Description

1.7 cm PlastiBell Circumcision Device

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.