Dynatron 25 Series 125B

FDA UDI

Class II (US FDA UDI)

by Dynatronics Corp.

Identity

Trade Name: Dynatron 25 Series 125B FDA UDI
Generic Name: Physical therapy ultrasound system FDA UDI
Model / Reference: D125B FDA UDI

Identifiers

Primary DI / UDI-DI: 10660584000147 FDA UDI
510(k) Number: K961250 FDA UDI
FDA Product Code: IMI FDA UDI
GMDN Term: Physical therapy ultrasound system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5300 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 — 4.0 Pound FDA UDI
Height — 4.0 Inch FDA UDI
Width — 7 Inch FDA UDI
Length — 9.0 Inch FDA UDI

Category: Physical therapy ultrasound system

Dynatron 25 Series 125B 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 222d13a3-7651-4e6a-b579-f03f34476b48 36 fields · synced Jun 8, 2026