Wall Expander (Side cutter)

FDA UDI

Class I (US FDA UDI)

by Dentis Co. , Ltd

Identity

Trade Name: Wall Expander (Side cutter) FDA UDI
Generic Name: Tissue expander injection port FDA UDI
Device Name: Dental Implant Instrument / Wall Expander (Side cutter) FDA UDI
Model / Reference: DSSWE FDA UDI
Description: Dental Implant Instrument / Wall Expander (Side cutter) FDA UDI

Identifiers

Primary DI / UDI-DI: 08806169146045 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Tissue expander injection port FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

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: Tissue expander injection port

Wall Expander (Side cutter) by Dentis Co. , Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Dentis Co. , Ltd

Sources (1)

FDA UDI 1d1d8b9d-15ab-43d8-97e9-39955abfdb50 33 fields · synced May 30, 2026