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PAPER POINT, Conventional type, XXF

Produits dentaires S.A. · Model 25976 · UDI-DI 08809264298701

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

Description

Used in root canal therapy to remove moisture from the root canal or to introduce medicaments Box of 200 - Type XXF

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.