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Jameson Tenotomy Scissors

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
JAMESON TENOTOMY SCISSORS FDA UDI
Generic Name
Tenotome FDA UDI
Device Name
JAMESON TENOTOMY SCISSORS CURVED BLADES FDA UDI
Model / Reference
2405-335 FDA UDI
Description
JAMESON TENOTOMY SCISSORS CURVED BLADES FDA UDI

Identifiers

Catalog Number
2405-335 FDA UDI
Primary DI / UDI-DI
00192896066601 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Tenotome FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 10.25 Inch FDA UDI

Category: Tenotome

Jameson Tenotomy Scissors by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tenotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4ac5c1ef-32e5-4154-ba0f-92bc3ba28f98 36 fields · synced Jun 6, 2026