Pincette

FDA UDI

Class I (US FDA UDI)

by POINTIMPLANT Co., Ltd.

Identity

Trade Name: Pincette FDA UDI
Generic Name: Dental implant/prosthesis handling forceps FDA UDI
Model / Reference: BIP FDA UDI

Identifiers

Primary DI / UDI-DI: 08800011266530 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Dental implant/prosthesis handling forceps 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

MRI Safety

MR Conditional FDA UDI

Category: Dental implant/prosthesis handling forceps

Pincette by POINTIMPLANT 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: POINTIMPLANT Co., Ltd.

Sources (1)

FDA UDI a0cc43a7-ee60-45dc-9e61-a11462c915ac 32 fields · synced May 30, 2026