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Iris

FDA UDI

Class I (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
IRIS FDA UDI
Generic Name
Manual dental scaler, reusable FDA UDI
Device Name
#13-14 AF Gracey Iris® Silicone Double End Curette FDA UDI
Model / Reference
4696-582 FDA UDI
Description
#13-14 AF Gracey Iris® Silicone Double End Curette FDA UDI

Identifiers

Primary DI / UDI-DI
00366975018854 FDA UDI
FDA Product Code
EMN FDA UDI
GMDN Term
Manual dental scaler, reusable 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

Yes

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

Dimensions & Sizes

Size
Length — 6.75 Inch FDA UDI

Category: Manual dental scaler, reusable

Iris by Benco Dental Supply Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual dental scaler, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96bc1759-f019-4b9c-8c2e-ab1092053045 35 fields · synced May 30, 2026