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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
Hand-held dental retractor FDA UDI
Device Name
WALLACE STIFLE RETRACTOR FDA UDI
Model / Reference
45-4955 FDA UDI
Description
WALLACE STIFLE RETRACTOR FDA UDI

Identifiers

Primary DI / UDI-DI
00817524028669 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Hand-held dental retractor 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: Hand-held dental retractor

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 Hand-held dental retractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b895ff13-47eb-46a4-b8da-ff3e66e9a802 33 fields · synced Jun 9, 2026