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KONG-TL VBR System, Inserter for VBR

FDA UDI

Class II (US FDA UDI)

by Icotec

Identity

Trade Name
KONG-TL VBR System, Inserter for VBR FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
KONG-TL VBR System, Inserter for VBR FDA UDI
Model / Reference
44-040 FDA UDI
Description
KONG-TL VBR System, Inserter for VBR FDA UDI

Identifiers

Catalog Number
44-040 FDA UDI
Primary DI / UDI-DI
07640164847832 FDA UDI
FDA Product Code
MQP FDA UDI
PLR FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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: Orthopaedic inorganic implant inserter/extractor, reusable

KONG-TL VBR System, Inserter for VBR by Icotec — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icotec

Sources (1)

  • FDA UDI 66a6b275-6be5-47ac-b4dc-cf0a3c4ed9ed 35 fields · synced Jun 8, 2026