Question 1

Who is the manufacturer of PULPDENT DENTAL BOND ENCHANCER?

Accepted Answer

Pulpdent Corp. filed the 510(k) submission for PULPDENT DENTAL BOND ENCHANCER (K926074).

Question 2

What is the FDA product code for PULPDENT DENTAL BOND ENCHANCER?

Accepted Answer

EBF. It is classified under 21 CFR 872.3690 as a Class 2 device in the Dental panel.

Question 3

When was PULPDENT DENTAL BOND ENCHANCER cleared by the FDA?

Accepted Answer

Mar 16, 1993 (decision: SESE).

Question 4

What is the regulatory pathway for PULPDENT DENTAL BOND ENCHANCER?

Accepted Answer

510(k) clearance (submission type: Traditional).

Question 5

Who can help prepare an FDA 510(k) submission like PULPDENT DENTAL BOND ENCHANCER?

Accepted Answer

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Record ID	K926074
Device Name	PULPDENT DENTAL BOND ENCHANCER
Applicant	Pulpdent Corp.
Product Code	EBF · Dental
Decision Date	Mar 16, 1993
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 872.3690
Device Class	Class 2

PULPDENT DENTAL BOND ENCHANCER

Device Facts

Regulatory Classification

Identification