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ERA® Slot Expander

FDA UDI

Class I (US FDA UDI)

by Sterngold Dental LLC

Identity

Trade Name
ERA® Slot Expander FDA UDI
Generic Name
Surgical torque wrench, reusable FDA UDI
Device Name
Used to widen the open space in dental attachment. Tool is made of stainless steel. FDA UDI
Model / Reference
905217 FDA UDI
Description
Used to widen the open space in dental attachment. Tool is made of stainless steel. FDA UDI

Identifiers

Primary DI / UDI-DI
00841549117930 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical torque wrench, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical torque wrench, reusable

ERA® Slot Expander by Sterngold Dental LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical torque wrench, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 583afbf4-6cbd-48d6-becd-b1e38dfe0e8c 34 fields · synced May 29, 2026