NEXUS

Cement, Dental

SYBRON DENTAL SPECIALTIES, INC.

The following data is part of a premarket notification filed by Sybron Dental Specialties, Inc. with the FDA for Nexus.

Pre-market Notification Details

• Device ID: K954762
• 510k Number: K954762
• Device Name: NEXUS
• Classification: Cement, Dental
• Applicant: SYBRON DENTAL SPECIALTIES, INC. 1332 SOUTH LONE HILL AVE. Glendora, CA 91740
• Contact: Jeffrey A Anderson
• Correspondent: Jeffrey A Anderson; SYBRON DENTAL SPECIALTIES, INC. 1332 SOUTH LONE HILL AVE. Glendora, CA 91740
• Product Code: EMA
• CFR Regulation Number: 872.3275 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-10-17
• Decision Date: 1995-11-02