RePlant® Precision IO Scan Adapter

FDA UDI

Class I (US FDA UDI)

by Implant Direct Sybron Manufacturing Llc

Identity

Trade Name: RePlant® Precision IO Scan Adapter FDA UDI
Generic Name: Dental guided surgery reference pin FDA UDI
Model / Reference: 6035-09PT FDA UDI

Identifiers

Catalog Number: 6035-09PT FDA UDI
Primary DI / UDI-DI: 10841307123934 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Dental guided surgery reference pin 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

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

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

Category: Dental guided surgery reference pin

RePlant® Precision IO Scan Adapter by Implant Direct Sybron Manufacturing Llc — 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: Implant Direct Sybron Manufacturing Llc

Sources (1)

FDA UDI eae86535-b334-4292-b871-6d2ad096d482 35 fields · synced Jun 8, 2026