Dr -hos

FDA UDI

Class I (US FDA UDI)

by Guangzhou Xinbo Electronic Co., Ltd.

Identity

Trade Name: DR -HOS FDA UDI
Generic Name: Knee support orthosis FDA UDI
Device Name: One knee joint support. Made of cloth, the device is worn on the body FDA UDI
Model / Reference: NN-KN-Blue FDA UDI
Description: One knee joint support. Made of cloth, the device is worn on the body FDA UDI

Identifiers

Primary DI / UDI-DI: 06970742221732 FDA UDI
FDA Product Code: MNE FDA UDI
GMDN Term: Knee support orthosis FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3475 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

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Knee support orthosis

Dr -hos by Guangzhou Xinbo Electronic Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Knee support orthosis.

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MEDI — MEDI MANUFACTURING, INC. · Class I
MEDI — MEDI MANUFACTURING, INC. · Class I
NON FRANCHISE — DJO, LLC · Class I
DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
Gripper Hinged Knee — MEDICAL SPECIALTIES INCORPORATED · Class I
DeRoyal — DEROYAL INDUSTRIES, INC. · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Guangzhou Xinbo Electronic Co., Ltd.

Sources (1)

FDA UDI 889f7a04-ea06-46b4-9f58-826347607973 33 fields · synced May 30, 2026