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Comfort Plus Osteotome

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
Comfort Plus Osteotome FDA UDI
Generic Name
Orthopaedic osteotome FDA UDI
Device Name
Comfort Plus Osteotome 30mm Curved 16.5cm Handles 29cm Total Length FDA UDI
Model / Reference
7532-30 FDA UDI
Description
Comfort Plus Osteotome 30mm Curved 16.5cm Handles 29cm Total Length FDA UDI

Identifiers

Catalog Number
7532-30 FDA UDI
Primary DI / UDI-DI
10840199528759 FDA UDI
FDA Product Code
KDG FDA UDI
GMDN Term
Orthopaedic osteotome FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic osteotome

Comfort Plus Osteotome by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic osteotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI fbc9556c-d5b5-4f5c-9292-601c91d97a82 36 fields · synced May 30, 2026