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DiamoDent

FDA UDI

Class I (US FDA UDI)

by Diamodent

Identity

Trade Name
DiamoDent FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Cap for Latch Driver Tip FDA UDI
Model / Reference
N/A FDA UDI
Description
Cap for Latch Driver Tip FDA UDI

Identifiers

Catalog Number
T5491 FDA UDI
Primary DI / UDI-DI
D907T54910 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

No

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
Dry Heat Sterilization FDA UDI

Category: Surgical instrument handle, non-torque-limiting

DiamoDent by Diamodent — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamodent

Sources (1)

  • FDA UDI 2ded7f62-f81c-44ff-9aa1-46f6ba4f408e 34 fields · synced Jun 1, 2026