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Osteotomes Kit

FDA UDI

Class I (US FDA UDI)

by Dentin Implants Technologies Ltd

Identity

Trade Name
OSTEOTOMES KIT FDA UDI
Generic Name
Dental osteotome set FDA UDI
Device Name
Straight Osteotomes kit FDA UDI
Model / Reference
SMB-T001 FDA UDI
Description
Straight Osteotomes kit FDA UDI

Identifiers

Primary DI / UDI-DI
07290113356023 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental osteotome set 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental osteotome set

Osteotomes Kit by Dentin Implants Technologies Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental osteotome set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d32e3bc-a186-4845-9858-bd54147adfc7 33 fields · synced May 30, 2026