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Optimized Ortho Positioning (OPS) Femoral

FDA UDI

Class II (US FDA UDI)

by Optimized Ortho Pty Ltd

Identity

Trade Name
Optimized Ortho Positioning (OPS) Femoral FDA UDI
Generic Name
Custom-made orthopaedic/craniofacial surgical guide FDA UDI
Device Name
Patient Specific Femoral Guide FDA UDI
Model / Reference
1250-1100 FDA UDI
Description
Patient Specific Femoral Guide FDA UDI

Identifiers

Primary DI / UDI-DI
09351327000039 FDA UDI
FDA Product Code
PBF FDA UDI
LWJ FDA UDI
MEH FDA UDI
LZO FDA UDI
GMDN Term
Custom-made orthopaedic/craniofacial surgical guide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3360 FDA UDI
888.3353 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Custom-made orthopaedic/craniofacial surgical guide

Optimized Ortho Positioning (OPS) Femoral by Optimized Ortho Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made orthopaedic/craniofacial surgical guide.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Optimized Ortho Pty Ltd

Sources (1)

  • FDA UDI 22086808-05b1-4e77-8692-bac7cff334f2 33 fields · synced Jun 8, 2026