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Diamond Orthopedic, LLC

FDA UDI

Class I (US FDA UDI)

by Diamond Orthopedic

Identity

Trade Name
Diamond Orthopedic, LLC FDA UDI
Generic Name
Surgical countersink, reusable FDA UDI
Device Name
Countersink - cannulated, for 2.4mm cannulated screws FDA UDI
Model / Reference
DMD-310-803 FDA UDI
Description
Countersink - cannulated, for 2.4mm cannulated screws FDA UDI

Identifiers

Catalog Number
DMD-310-803 FDA UDI
Primary DI / UDI-DI
B551DMD310803 FDA UDI
FDA Product Code
HWW FDA UDI
GMDN Term
Surgical countersink, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical countersink, reusable

Diamond Orthopedic, LLC by Diamond Orthopedic — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical countersink, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamond Orthopedic

Sources (1)

  • FDA UDI 411cbda5-ec98-4a64-adf0-f6d37433bbc5 35 fields · synced May 30, 2026