Overdenture Abutment Plastic Transfer (2 pieces)

FDA UDI

Class I (US FDA UDI)

by Implant Direct Sybron Manufacturing Llc

Identity

Trade Name: Overdenture Abutment Plastic Transfer (2 pieces) FDA UDI
Generic Name: Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Model / Reference: 1000-68 FDA UDI

Identifiers

Catalog Number: 1000-68 FDA UDI
Primary DI / UDI-DI: 10841307120988 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Overdenture Abutment Plastic Transfer (2 pieces) by Implant Direct Sybron Manufacturing Llc — Class I — FDA UDI — listed in FDA GUDID

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Implant Direct Sybron Manufacturing Llc

Sources (1)

FDA UDI c1955d32-4b2c-46b6-9047-d19b5aae68f6 35 fields · synced May 30, 2026