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Vertical Anchor

FDA UDI

Class I (US FDA UDI)

by POINTIMPLANT Co., Ltd.

Identity

Trade Name
Vertical Anchor FDA UDI
Generic Name
Dental implantation drilling template stabilization bolt FDA UDI
Model / Reference
NVA2010L FDA UDI

Identifiers

Primary DI / UDI-DI
08800011266608 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation drilling template stabilization bolt 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Dental implantation drilling template stabilization bolt

Vertical Anchor by POINTIMPLANT Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation drilling template stabilization bolt.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
POINTIMPLANT Co., Ltd.

Sources (1)

  • FDA UDI 78d50222-bdcf-4278-8495-244197664016 32 fields · synced May 30, 2026