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Dynatron Solaris Plus 705

FDA UDI

Class II (US FDA UDI)

by Dynatronics Corp.

Identity

Trade Name
Dynatron Solaris Plus 705 FDA UDI
Generic Name
Multi-modality physical therapy system, professional-use FDA UDI
Model / Reference
D715T FDA UDI

Identifiers

Primary DI / UDI-DI
10660584000055 FDA UDI
510(k) Number
K031329 FDA UDI
FDA Product Code
LIH FDA UDI
IPF FDA UDI
ILY FDA UDI
GZJ FDA UDI
GMDN Term
Multi-modality physical therapy system, professional-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
890.5850 FDA UDI
890.5500 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 8.2 Pound FDA UDI
Height — 4.0 Inch FDA UDI
Width — 18.5 Inch FDA UDI
Length — 12.0 Inch FDA UDI

Category: Multi-modality physical therapy system, professional-use

Dynatron Solaris Plus 705 by Dynatronics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality physical therapy system, professional-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynatronics Corp.

Sources (1)

  • FDA UDI 0f100ac5-2d9c-46cd-828f-e2da224d16af 36 fields · synced Jun 8, 2026