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J&J Instruments

FDA UDI

Class I (US FDA UDI)

by J&J Instruments, LLC

Identity

Trade Name
J&J Instruments FDA UDI
Generic Name
Dental restoration carver, resin FDA UDI
Device Name
CLEOID DISCOID #3/6 LARGE FDA UDI
Model / Reference
04-603 FDA UDI
Description
CLEOID DISCOID #3/6 LARGE FDA UDI

Identifiers

Primary DI / UDI-DI
00817524021509 FDA UDI
FDA Product Code
EIK FDA UDI
GMDN Term
Dental restoration carver, resin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental restoration carver, resin

J&J Instruments by J&J Instruments, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restoration carver, resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3618862c-3d3b-41ed-ac6a-1a1ddafd7323 33 fields · synced Jun 9, 2026