Fomon nasal scissors

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name: Fomon nasal scissors FDA UDI
Generic Name: Nasal scissors FDA UDI
Device Name: curved, double blade 12 cm FDA UDI
Model / Reference: 20-633-12 FDA UDI
Description: curved, double blade 12 cm FDA UDI

Identifiers

Catalog Number: 20-633-12 FDA UDI
Primary DI / UDI-DI: 04250381855713 FDA UDI
FDA Product Code: KBD FDA UDI
GMDN Term: Nasal scissors FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Nasal scissors

Fomon nasal scissors are a cutting-edge medical device designed for precise and delicate surgeries in the ear, nose, and throat (ENT) region. Made from high-grade stainless steel, these hand-held instruments feature two pivoted blades with finger and thumb rings, allowing for a shearing action that cuts tissue effectively. The device is available in various designs and sizes, including slender, pointed blades and carbide inserts, making it suitable for both general and plastic surgery procedures.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Spiggle & Theis Medizintechnik GmbH

Sources (1)

FDA UDI a5260b0d-14ff-47e4-aa97-5d7be83185f0 35 fields · synced Jul 23, 2026