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Snucone Bone Level Implant System

FDA UDI

Class II (US FDA UDI)

by SNUCONE Co., LTD.

Identity

Trade Name
SNUCONE BONE LEVEL IMPLANT SYSTEM FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Model / Reference
AF+B-5807S FDA UDI

Identifiers

Primary DI / UDI-DI
08800020854735 FDA UDI
510(k) Number
K210354 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Screw endosteal dental implant, two-piece

Snucone Bone Level Implant System by SNUCONE Co., LTD. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SNUCONE Co., LTD.

Sources (1)

  • FDA UDI 8df029a9-7ee7-4609-ba30-bc2a3c189ce6 34 fields · synced May 30, 2026