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HoMedics

FDA UDI

Class I (US FDA UDI)

by Fka Distributing Co., Llc

Identity

Trade Name
HoMedics FDA UDI
Generic Name
Inversion table FDA UDI
Device Name
Compact Inversion back stretcher FDA UDI
Model / Reference
BM-IS500J FDA UDI
Description
Compact Inversion back stretcher FDA UDI

Identifiers

Primary DI / UDI-DI
00031262113733 FDA UDI
FDA Product Code
INW FDA UDI
GMDN Term
Inversion table FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3750 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inversion table

HoMedics by Fka Distributing Co., Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 441d3f21-2d42-48f6-9b67-a19cd8637569 33 fields · synced Jun 8, 2026