Synchrony Dysphagia Solutions by ACP

FDA UDI

Class II (US FDA UDI)

by Accelerated Care Plus Corp.

Identity

Trade Name: Synchrony Dysphagia Solutions by ACP FDA UDI
Generic Name: Bioelectrical signal analysis software FDA UDI
Device Name: Bioelectrical signal analysis software; Biomechanical function analysis, interactive rehabilitation system FDA UDI
Model / Reference: 300800A FDA UDI
Description: Bioelectrical signal analysis software; Biomechanical function analysis, interactive rehabilitation system FDA UDI

Identifiers

Primary DI / UDI-DI: 00858703006337 FDA UDI
FDA Product Code: GXY FDA UDI
ION FDA UDI
HCC FDA UDI
GMDN Term: Bioelectrical signal analysis software FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1320 FDA UDI
890.5370 FDA UDI
882.5050 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

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Bioelectrical signal analysis software

Synchrony Dysphagia Solutions by ACP by Accelerated Care Plus 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: Accelerated Care Plus Corp.

Sources (1)

FDA UDI a6816098-d95f-42fb-8e7a-b221982f2430 34 fields · synced May 30, 2026