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Eleos™

FDA UDI

Class III (US FDA UDI)

by Onkos Surgical, Inc.

Identity

Trade Name
ELEOS™ FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
FEMORAL HEAD, SUPER FINISH36MM TAPER, +3.5MM 36MM, +3.5MM FDA UDI
Model / Reference
26000027E FDA UDI
Description
FEMORAL HEAD, SUPER FINISH36MM TAPER, +3.5MM 36MM, +3.5MM FDA UDI

Identifiers

Catalog Number
26000027E FDA UDI
Primary DI / UDI-DI
B27826000027E0 FDA UDI
510(k) Number
K161520 FDA UDI
FDA Product Code
JDL FDA UDI
KWA FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3320 FDA UDI
888.3330 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

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Metallic femoral head prosthesis

Eleos™ by Onkos Surgical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 195a03e3-9cd3-4273-ab71-8f3d4a2bf4e1 36 fields · synced Jun 6, 2026