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XP-4D

Peter Brasseler Holdings, LLC · Model 5031705U0 · UDI-DI 08404535012231

EKN Prescription
7
510(k) clearances
0
Adverse events
5
Recalls
86
Facilities

Description

XP-4D ABSORBENT PP STARTER 100P

Recalls

DateFirmReason
2017-08-04Ultradent Products, Inc.The barcode label was placed underneath the sterile barrier and the product was re-wrapped.
2017-08-04Ultradent Products, Inc.The barcode label was placed underneath the sterile barrier and the product was re-wrapped.
2017-08-04Ultradent Products, Inc.The barcode label was placed underneath the sterile barrier and the product was re-wrapped.
2017-08-04Ultradent Products, Inc.The barcode label was placed underneath the sterile barrier and the product was re-wrapped.
2017-08-04Ultradent Products, Inc.The barcode label was placed underneath the sterile barrier and the product was re-wrapped.

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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.