Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: NPL FDA class 2

Barrier, Animal Source, Intraoral

Dental

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The animal-source intraoral barrier is a dental implant device made of animal-derived materials such as collagen, intended to aid in guided tissue and bone regeneration procedures and to act as a stable barrier for containment of bone graft materials around implants. It is classified as FDA Class 2 under regulation 872.3930 in the Dental specialty, requiring 510(k) clearance, and carries an implant flag. Product code NPL is not eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
SwissMembrane X; SwissMembrane X Socket
Soft Tissue Augmentation Resorbable Matrix
Oral Matrix
Endoform Dental Membrane
THE Cover
InterCollagen® Guide
Kerecis Oral
OSSIX Breeze
Geistlich Bio-Gide, Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed, Geistlich Bio-Gide Perio, Geistlich Combi-Kit Collagen and Geistlich Perio-System Combi Pack
Geistlich Mucograft®, Geistlich Mucograft® Seal
Striate+™
Kerecis Gingiva Graft
OssGuide
Geistlich Bio-Gide, Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed, Geistlich Bio-Gide Perio, Geistlich Combi-Kit Collagen, Geistlich Perio-System Combi-Pack, Geistlich Mucograft and Geistlich Mucograft Seal
Straumann Jason Membrane
Geistlich Fibro-Gide
Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed
DynaMatrix/Dynamatrix Plus
OSSIX VOLUMAX
OSSIX PLUS
DSM Biomedical Porcine Pericardium Dental Membrane
VITALA PORCINE DERIVED COLLAGEN MEMBRANE
Collagen Dental Membrane - Conformable IIBP
COLLAGEN DENTAL MEMBRANE - CONFORMABLE PP
GUIDOSS
GEISTLICH MUCOGRAFT: 15 X 20 MM, 20 X 30 MM, 8 MM DIAMETER
MATRICEL DENTAL BARRIER MEMBRANE
MESOTHELIUM DENTAL MEMBRANE
COLLADENTAL BARRIER
COVAMAX RESORBABLE COLLAGEN MEMBRANE
COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN
VITALA NATURAL RESORBABLE COLLAGEN MEMBRANE
GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS
MUCOGRAFT
COLLAGEN DENTAL MEMBRANE V
KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX
KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANE
COLLAGEN DENTAL MEMBRANE IV
DYNAMATRIX
OTA COLLAGEN BIOMATERIAL
MUCOGRAFT COLLAGEN MATRIX
TUTODENT DENTAL MEMBRANE
FORTAGEN ORAL MEMBRANE
COLLAGEN DENTAL MEMBRANE III
COLLAGEN DENTAL MENBRANE - CONFORMABLE II
MUCOGRAFT
OSSIX -PLUS
BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE
BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE REGENERATION
MUCOGRAFT

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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