K.T.Surgico

FDA UDI

Class I (US FDA UDI)

by K.t.surgico

Identity

Trade Name: K.T.Surgico FDA UDI
Generic Name: General-purpose surgical scissors, single-use FDA UDI
Device Name: LITTAUER STITCH SCISSORS 4.5" STR FDA UDI
Model / Reference: 2023 FDA UDI
Description: LITTAUER STITCH SCISSORS 4.5" STR FDA UDI

Identifiers

Catalog Number: KTS0880111 FDA UDI
Primary DI / UDI-DI: KTS0880111 FDA UDI
FDA Product Code: LRW FDA UDI
GMDN Term: General-purpose surgical scissors, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose surgical scissors, single-use

K.T.Surgico by K.t.surgico — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical scissors, single-use.

Bioseal Inc. — BIOSEAL · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Sklar — Sklar Corporation · Class I
Centurion — Centurion Medical Products · Class I
Sklar® — Sklar Corporation · Class I
Bioseal Inc. — BIOSEAL · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Sklar — Sklar Corporation · Class I

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: K.t.surgico

Sources (1)

FDA UDI 7b4aaf32-0114-4a10-a145-cb8e38a5f6a3 36 fields · synced Jun 1, 2026