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Locking cage

FDA UDI

Class II (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name
Locking cage FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Locking cage tray #2 FDA UDI
Model / Reference
9208-8120 FDA UDI
Description
Locking cage tray #2 FDA UDI

Identifiers

Catalog Number
9208-8120 FDA UDI
Primary DI / UDI-DI
04719872142324 FDA UDI
510(k) Number
K163441 FDA UDI
FDA Product Code
LZO FDA UDI
JDI FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Locking cage by United Orthopedic Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

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 4ce14d67-5a4c-458a-9e7a-95144981967d 36 fields · synced May 31, 2026