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: NPM FDA class 2

Bone Grafting Material, Animal Source

Dental

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The animal-source bone grafting material for dental use is a naturally derived device such as collagen intended to fill, augment, or reconstruct periodontal or jaw bone defects following disease, trauma, or surgery. 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 NPM is not eligible for third-party review.

510(k) Clearances

39 matches
K Number
Device Name
Geistlich Bio-Oss®; Geistlich Bio-Oss Pen®
SwissGraft X
Geistlich Bio-Flow®
Xenograft Bovine Bone Particulate
THE Graft Collagen
Geistlich Bio-Oss®
S1
InterOss Collagen
Wishbone HA
Porcine Mineral Collagen Composite
Porcine Mineral Collagen Composite Moldable
DSM Biomedical Dental Bone Graft Plus
The Graft Bone Substitute
Straumann cerabone
The Graft Natural Bone Substitute
Anorganic Bone Mineral with Collagen in Delivery Applicator
OSSIX BONE
Anorganic Bone Mineral in Delivery Applicator
DSM Biomedical Dental Bone Graft
Porcine Anorganic Bone Mineral in Delivery Applicator
A-Oss
Regenomer® Syringe, Regenomer® Plug, Regenomer® Block
InterOss
OCS-B COLLAGEN
TI-OSS
PORCINE ANORGANIC BONE MINERAL
SYNERGY
GEISTLICH BIO-OSS, GEISTLICH BIO-OSS COLLAGEN, GEISTLICH COMBI-KIT COLLAGEN, GEISTLICH PERIO SYSTEM COMBI PACK, GEISTLIC
OCS-B
CERASORB PLUS
GEISTLICH BIO-OSS PEN (0.25 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-OSS PEN (0.5 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-O
GEISTLICH COMBI-KIT COLLEGEN
GEISTLICH PERIO-SYSTEM COMBI-PACK , GEISTLICH BIO-GIDE PERIO
EQUIMATRIX
OSTA MAXIGRO AND REGIGRO
BIO-OSS COLLAGEN
OSTEOTAPE
OSTEOGUIDE ANORGANIC BONE MINERAL PRODUCTS
BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN

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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