J & J Instruments Inc

FDA UDI

Class I (US FDA UDI)

by J&J Instruments, LLC

Identity

Trade Name: J & J INSTRUMENTS INC FDA UDI
Generic Name: Dental excavator, reusable FDA UDI
Device Name: CAVITY LINER 6"" DE REG/LONG FDA UDI
Model / Reference: 02-550 FDA UDI
Description: CAVITY LINER 6"" DE REG/LONG FDA UDI

Identifiers

Catalog Number: 02-550 FDA UDI
Primary DI / UDI-DI: 00817524020786 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: Dental excavator, 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

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Length — 5.875 Inch FDA UDI

Category: Dental excavator, reusable

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

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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

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Manufacturer

Manufacturer: J&J Instruments, LLC

Sources (1)

FDA UDI 3e456591-f817-4a92-8f97-fb61cc9b5052 35 fields · synced Jun 9, 2026