Dynatron SmarTRAC

FDA UDI

Class II (US FDA UDI)

by Dynatronics Corp.

Identity

Trade Name: Dynatron SmarTRAC FDA UDI
Generic Name: Intermittent powered traction system FDA UDI
Model / Reference: DSTC1 FDA UDI

Identifiers

Primary DI / UDI-DI: 10660584000451 FDA UDI
510(k) Number: K151640 FDA UDI
FDA Product Code: ITH FDA UDI
GMDN Term: Intermittent powered traction system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5900 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Weight — 22 Pound FDA UDI
Width — 11.8 Inch FDA UDI
Length — 13.4 Inch FDA UDI
Height — 8.7 Inch FDA UDI

Category: Intermittent powered traction system

Dynatron SmarTRAC by Dynatronics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Dynatronics Corp.

Sources (1)

FDA UDI 5bad2b6e-7624-4b5f-8e8f-ede489c3bbb3 36 fields · synced Jun 8, 2026