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Implant Hand Piece Driver

FDA UDI

Class I (US FDA UDI)

by Surgikor, LLC

Identity

Trade Name
Implant Hand Piece Driver FDA UDI
Generic Name
Basket endosteal dental implant, two-piece FDA UDI
Device Name
Implant Hand Piece Driver Conical RP Long FDA UDI
Model / Reference
MMDCRP02026 FDA UDI
Description
Implant Hand Piece Driver Conical RP Long FDA UDI

Identifiers

Primary DI / UDI-DI
D824MMDCRP020260 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Basket endosteal dental implant, two-piece 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

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

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: Basket endosteal dental implant, two-piece

Implant Hand Piece Driver by Surgikor, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basket endosteal dental implant, two-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgikor, LLC

Sources (1)

  • FDA UDI 5c81b088-0893-43da-a28c-c3a06cd6894c 33 fields · synced May 30, 2026