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: MIB FDA class 2

Elastomer, Silicone Block

Ear, Nose, Throat

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The Silicone Block Elastomer is a solid silicone material used as a building block or filler implant in otolaryngology and head-and-neck reconstructive surgery, such as augmenting or reconstructing soft tissue structures in the ear, nose, or throat regions. Classified as a Class 2 implantable device under 21 CFR 874.3620 within the Ear, Nose, and Throat specialty, it requires 510(k) premarket notification. It carries an implant flag, indicating it is intended to be placed inside the body.

510(k) Clearances

45 matches
K Number
Device Name
MISTI Silicone Implant
Pre-Formed Silicone Block
ShiNeo Silicone Implant
AugMENTA Penile Implant
Pre-Formed Penile Silicone Block
BioSiCar Silicone Implant
Pre-Formed Penile Silicone Block
SOFTXIL
Pre-Formed Penile Silicone Block
GLUTEAL IMPLANT, MODELS RND 5-X, TRD 6-X
CALF IMPLANT, MODEL EC17-X
SILIMED PECTORAL IMPLANT
SILICONE BLOCK
MEDISIL SILICONE SHEETING
HANSON MEDICAL GLUTEAL IMPLANT
HANSON MEDICAL CALF IMPLANT
AART CALF IMPLANT
AART SILICONE SHEETING
AART GLUTEAL IMPLANT
AART SILICONE CARVING BLOCK
SEARE BIOMEDICAL SILICONE RODS
SPECTRUM DESIGNS PRE-FORM CONTOUR SILICONE CARVING BLOCK
SEARE BIOMEDICAL SILICONE SHEETING
STERILE SILICONE EXTERNAL WOUND COVER
SILIMED SILICONE CARVING BLOCK
SILICONE ELASTOMER SHEETING
SILIMED CALF IMPLANT
SILICONE BLOCKS
SILIMED GLUTEAL IMPLANT
DURASIL I AND DURASIL II
DOW CORNING SILASTIC ELASTOMER Q7-4750
SILICONE CARVING BLOCK
DURALASTIC I AND DURALASTIC II
SIL-TEC SMALL/LARGE BORE TUBING/SIL-TEC HIGH DUROMETER TUBING/SIL-TEC RADIOPAQUE TUBING
SPIRIT RIDGE SILICONE CARVING BLOCK
DURALASTIC SHEETING II
SPECTRUM DESIGNS SILICONE BLOCK
DURALASTIC I
DURALASTIC II
PROLASTIC SHEETING
MEDICAL GRADE SILICONE BLOCK
DURALASTIC SHEETING
DURALASTIC SHEETING
IMPLANTECH MEDICAL GRADE SILICONE SHEETING
ZARA SILICONE BLOCK

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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