FDA.reportPublic FDA data

Cartilage Graft Cutter

Primary DI
00192896122499
Brand
Cartilage Graft Cutter
Company
SONTEC INSTRUMENTS, INC.
Model
350-842
Catalog number
350-842
Device description
Cartilage Graft Cutter
Published
2025-11-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FZTCUTTER, SURGICAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FZTCutter, SurgicalGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00192896122499PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00192896122499001928961224991928961224990192896122499

GMDN Terms#

Term, Definition table
TermDefinition
ENT cartilage cutterA portable, manual surgical instrument intended to cut a harvested cartilage specimen (e.g., tragus-derived autograft) to an accurate predetermined thickness for patient implantation during an ear/nose/throat (ENT) procedure (e.g., middle ear surgery). It typically consists of an adjustable cutting assembly with a handle, base, and thickness dial used in conjunction with a removable ENT cartilage cutter blade. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Dry Heat Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800)821-7496info@sontecinstruments.com

Regulatory Flags#

DUNS number
040729840
Device count
1
Premarket exempt
true
Lot or batch
true
No natural rubber latex
true
Sterilization required before use
true

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00192896015296ENUCLEATION SCISSORS13-982013-98202018-09-13
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