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J&J Instruments, LLC

United States·US-MF-000008974

Last updated September 17, 2026

About

Our instructions on how to clean and properly care for your J&J Instruments, click here for more info »

From the manufacturer's own website. Source

What J&J Instruments, LLC makes

J&J Instruments, LLC manufactures a range of reusable dental and surgical instruments. Their product portfolio includes manual dental scalers, dental surgical scissors, tooth extraction forceps, orthodontic pliers, periosteal elevators, suturing needle holders, and dental surgical probes.

The company is based in the United States and produces devices categorized as Class I and Class II medical devices. These products are listed in the FDA UDI database.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does J&J Instruments, LLC manufacture?

J&J Instruments, LLC specializes in reusable dental and surgical instruments. Their product line includes manual dental scalers, dental surgical scissors, tooth extraction forceps, orthodontic pliers, periosteal elevators, suturing needle holders, and dental surgical probes. These devices are designed for use in dental and surgical procedures.

Where is J&J Instruments, LLC based?

J&J Instruments, LLC is headquartered in the United States. The company’s location is relevant for regulatory purposes, as it operates under the jurisdiction of the U.S. Food and Drug Administration (FDA).

Which regulatory registries list J&J Instruments, LLC’s devices?

J&J Instruments, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for medical devices authorized in the U.S., helping healthcare providers and regulators verify product details.

How are J&J Instruments, LLC’s devices classified under FDA regulations?

J&J Instruments, LLC’s devices fall into two primary FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. Classification depends on factors like intended use and potential health impact.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
120, Goodwin Place, Stratford, United States
LinkedIn
—
Facebook
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Phone
+01 908-587-1021
PRRC Contact
Scott Philhower
EUDAMED SRN
US-MF-000008974
FDA FEI Number
—
DUNS Number
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Catalogue (1079)

Page 22 of 22
DeviceModel / ReferenceRegistriesClassStatus
Julius Wirth 736-011
EUDAMED
Class IActive
Julius Wirth 201-002
EUDAMED
Class IActive
Julius Wirth 725-001
EUDAMED
Class IActive
Julius Wirth 104-002
EUDAMED
Class IActive
Julius Wirth 206-007
EUDAMED
Class IActive
Julius Wirth 736-001
EUDAMED
Class IActive
Julius Wirth 735-002
EUDAMED
Class IActive
Julius Wirth 721-001
EUDAMED
Class IActive
Julius Wirth 402-011
EUDAMED
Class IActive
Julius Wirth 206-005
EUDAMED
Class IActive
Julius Wirth 405-032
EUDAMED
Class IActive
Julius Wirth 405-011
EUDAMED
Class IActive
Julius Wirth 736-005
EUDAMED
Class IActive
Julius Wirth 405-029
EUDAMED
Class IActive
Julius Wirth 104-007
EUDAMED
Class IActive
Julius Wirth 737-003
EUDAMED
Class IActive
Julius Wirth 605-006
EUDAMED
Class IActive
Julius Wirth 726-005
EUDAMED
Class IActive
Julius Wirth 506-002
EUDAMED
Class IActive
Julius Wirth 602-004
EUDAMED
Class IActive
Julius Wirth 602-003
EUDAMED
Class IActive
Julius Wirth 608-001
EUDAMED
Class IActive
Julius Wirth 405-042
EUDAMED
Class IActive
Julius Wirth 205-001
EUDAMED
Class IActive
Julius Wirth 603-002
EUDAMED
Class IActive
Julius Wirth 702-001
EUDAMED
Class IActive
Julius Wirth 203-016
EUDAMED
Class IActive
Julius Wirth 736-007
EUDAMED
Class IActive
Julius Wirth 101-003
EUDAMED
Class IActive

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