Klassic ONE Stem Trial Caddy for PS-Max Stem + Augment Instrument Tray

FDA UDI

Class I (US FDA UDI)

by Total Joint Orthopedics, Inc.

Identity

Trade Name: Klassic ONE Stem Trial Caddy for PS-Max Stem + Augment Instrument Tray FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: Stem Trial Caddy for PS-Max Stem + Augment Instrument Tray FDA UDI
Model / Reference: 2414.00.100 FDA UDI
Description: Stem Trial Caddy for PS-Max Stem + Augment Instrument Tray FDA UDI

Identifiers

Primary DI / UDI-DI: 00810094691899 FDA UDI
FDA Product Code: OJH FDA UDI
GMDN Term: Instrument tray, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Klassic ONE Stem Trial Caddy for PS-Max Stem + Augment Instrument Tray by Total Joint Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Instrument tray, reusable.

MİKRO — SAMSUN MİKRO CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ · Class I
Hu-Friedy — Hu-Friedy Manufacturing Co., LLC · Class I
Instrument Case — Katena Products, Inc. · Class I
Hu-Friedy — Hu-Friedy Manufacturing Co., LLC · Class I
MİKRO — SAMSUN MİKRO CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ · Class I
SHEFFIELD RING FIXATOR — Orthofix, Inc. · Class II
MİKRO — SAMSUN MİKRO CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ · Class I
ASELTECH — Asel Tibbi Aletler A.S. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: Total Joint Orthopedics, Inc.

Sources (1)

FDA UDI c7cf0957-67eb-45a5-8cad-21a1a62f16ff 35 fields · synced May 30, 2026