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Stoma®

FDA UDI

Class I (US FDA UDI)

by Storz am Mark GmbH

Identity

Trade Name
STOMA® FDA UDI
Generic Name
Periodontal knife FDA UDI
Device Name
Soft tissue splitter, Steigmann, edgeless, curved, DE FDA UDI
Model / Reference
14450.01 FDA UDI
Description
Soft tissue splitter, Steigmann, edgeless, curved, DE FDA UDI

Identifiers

Catalog Number
14450.01 FDA UDI
Primary DI / UDI-DI
ESAM14450011 FDA UDI
FDA Product Code
EMO FDA UDI
GMDN Term
Periodontal knife FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Periodontal knife

Stoma® by Storz am Mark GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periodontal knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Storz am Mark GmbH

Sources (1)

  • FDA UDI d506ca7d-c0e0-4982-8f04-39706b3cc114 35 fields · synced May 30, 2026