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Smart Correction

FDA UDI

Class I (US FDA UDI)

by Wishbone Medical Inc.

Identity

Trade Name
Smart Correction FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Strut Case Lid FDA UDI
Model / Reference
SC-STR-02 FDA UDI
Description
Strut Case Lid FDA UDI

Identifiers

Catalog Number
SC-STR-02 FDA UDI
Primary DI / UDI-DI
B562SCSTR020 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Smart Correction by Wishbone Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d46406a-3f59-4565-8c6f-1c1bca1afc98 36 fields · synced Jun 8, 2026