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: Orthodontic ligature director FDA UDI
Device Name: LIGATURE DIRECTOR SE HOLLOW FDA UDI
Model / Reference: 77-810 FDA UDI
Description: LIGATURE DIRECTOR SE HOLLOW FDA UDI

Identifiers

Primary DI / UDI-DI: 00817524029420 FDA UDI
FDA Product Code: ECP FDA UDI
GMDN Term: Orthodontic ligature director 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

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthodontic ligature director

J & J Instruments 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 a6c502a4-a148-4481-a90d-3f41edefa892 33 fields · synced Jun 9, 2026