← Back to catalogue

Diamond Orthopedic, LLC

FDA UDI

Class II (US FDA UDI)

by Diamond Orthopedic

Identity

Trade Name
Diamond Orthopedic, LLC FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
3.5mm, Cannulated Screw, Partially Thd., 28mm FDA UDI
Model / Reference
DMD-205-028 FDA UDI
Description
3.5mm, Cannulated Screw, Partially Thd., 28mm FDA UDI

Identifiers

Catalog Number
DMD-205-028 FDA UDI
Primary DI / UDI-DI
B551DMD2050280 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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: Orthopaedic bone screw, non-bioabsorbable, non-sterile

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

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Diamond Orthopedic

Sources (1)

  • FDA UDI 5ff500e8-3f80-4378-a1d4-4778ea4a8dcb 35 fields · synced Jun 8, 2026