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Single Arch Dam Conversion Kit 1PK

FDA UDI

Class I (US FDA UDI)

by Smart Denture Conversions, Llc

Identity

Trade Name
Single Arch Dam Conversion Kit 1PK FDA UDI
Generic Name
Denture clasp, polymer, preformed FDA UDI
Model / Reference
SADCK1PK FDA UDI

Identifiers

Primary DI / UDI-DI
D990SADCK1PK0 FDA UDI
FDA Product Code
NDP FDA UDI
EIE FDA UDI
GMDN Term
Denture clasp, polymer, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
872.6300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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: Surgical support tape, non-bioabsorbableRubber dam, non-latexDenture clasp, polymer, preformed

Single Arch Dam Conversion Kit 1PK by Smart Denture Conversions, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture clasp, polymer, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 446c1bae-4b9c-4043-a42a-1f0f40826a2c 32 fields · synced May 30, 2026