Nugent Forcep 30-10590-02

GUDID G2023010590021

Nugent forceps are a type of dental instrument that is used to grasp and manipulate tissues in the oral cavity. These forceps are named after Dr. James Nugent, a prominent dentist who developed the instrument in the 1930s. Nugent forceps feature a long, slender shaft with a curved, pointed tip at the end. The tip is designed to fit into the small spaces between teeth and gums, allowing the dentist to grasp and hold tissue while performing various procedures, such as scaling, root planing, or extraction. The forceps are typically made of high-quality stainless steel, which is durable, corrosion-resistant, and easy to clean and sterilize. Some models may have a serrated or textured tip for improved grip. Nugent forceps are commonly used in periodontal procedures, which focus on the health and treatment of the tissues that surround and support the teeth. These forceps can help the dentist to gently and effectively remove calculus and plaque from the teeth and gums, improving overall oral health. As with all dental instruments, proper care and maintenance are essential to ensure the longevity and effectiveness of Nugent forceps. The instrument must be cleaned and sterilized between uses to prevent the spread of infection, and it should be inspected regularly for signs of damage or wear.

CONCISE ENTERPRISES

Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: G2023010590021
• NIH Device Record Key: 685b05cf-48a5-4d71-bb9e-5c092095759b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nugent Forcep
• Version Model Number: 301059002
• Catalog Number: 30-10590-02
• Company DUNS: 645816062
• Company Name: CONCISE ENTERPRISES
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G2023010590021 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

[G2023010590021]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-14
• Device Publish Date: 2023-04-06

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