← Back to catalogue

Fora

FDA UDI

Class II (US FDA UDI)

by Fora Care Inc.

Identity

Trade Name
FORA FDA UDI
Generic Name
Home healthcare information system application software FDA UDI
Device Name
TeleHealth System FDA UDI
Model / Reference
24/7 HEALTHVIEW FDA UDI
Description
TeleHealth System FDA UDI

Identifiers

Primary DI / UDI-DI
00816042014949 FDA UDI
510(k) Number
K083046 FDA UDI
FDA Product Code
DRG FDA UDI
GMDN Term
Home healthcare information system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2910 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Home healthcare information system application software

Fora by Fora Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home healthcare information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fora Care Inc.

Sources (1)

  • FDA UDI dbb0e06e-fc71-4fbd-80b6-f7a7b43d463b 34 fields · synced May 30, 2026