K923711 is an FDA 510(k) clearance for the PERIOFLEX TIP. Classified as Unit, Oral Irrigation (product code EFS), Class I - General Controls.
Submitted by Novadent, Ltd. (Jerusalem, IL). The FDA issued a Cleared decision on May 16, 1994 after a review of 658 days - an unusually long review period, suggesting complex equivalence evaluation.
This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6510 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Dental submissions.
View all Novadent, Ltd. devices