FDA Device Intelligence
HomeBeijing C-Root Dental Medical Devices Co., LTD. › C-Root

C-Root

Beijing C-Root Dental Medical Devices Co., LTD. · Model 0.5g · UDI-DI 06972902581663

KIF
1
510(k) clearances
703
Adverse events
2
Recalls
76
Facilities

Recalls

DateFirmReason
2016-08-31Ormco/SybronendoSybronEndo is recalling the Sealapex Xpress because it was labeled with an incorrect expiration date of 2017-11 while the syringe was labeled with the correct expiration date of 20
2009-02-23Sybron Dental SpecialtiesSybron Dental Specialties is initiating a recall on the Sealapex Xpress due to the presence of crystals in the catalyst. This crystallization may affect proper canal filling by pre

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.