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Omega

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
OMEGA FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Standard Lag Screw FDA UDI
Model / Reference
3362-5-085 FDA UDI
Description
Standard Lag Screw FDA UDI

Identifiers

Catalog Number
3362-5-085 FDA UDI
Primary DI / UDI-DI
07613327093018 FDA UDI
510(k) Number
K955306 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 85.0 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Omega by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 26a87e7f-559f-47ba-9e7b-d5d01cb1d07a 36 fields · synced May 30, 2026