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Sterling

FDA UDI

Class I (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
STERLING FDA UDI
Generic Name
Periodontal probe, reusable FDA UDI
Model / Reference
5116-938 FDA UDI

Identifiers

Primary DI / UDI-DI
00366975006790 FDA UDI
FDA Product Code
EIX FDA UDI
GMDN Term
Periodontal probe, 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Periodontal probe, reusable

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

Similar devices

Also classified as Periodontal probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI beee106a-56d4-48a0-a35b-48809e2d92d8 32 fields · synced May 30, 2026