← Back to catalogue

Prosthesis, Hawley Retainer, Palatal Expander, Spacer, Herbst, Nance HoldingArch

FDA UDI

Class N (US FDA UDI)

by Shenzhen Minghao Dentures Co., Ltd.

Identity

Trade Name
Prosthesis, Hawley Retainer, Palatal Expander, Spacer, Herbst, Nance HoldingArch FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Model / Reference
Not Applicable FDA UDI

Identifiers

Primary DI / UDI-DI
06970617030100 FDA UDI
FDA Product Code
NSR FDA UDI
GMDN Term
Orthodontic retainer FDA UDI

Classification

Device Class
N FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ultraviolet Light FDA UDI

Category: Orthodontic retainer

Prosthesis, Hawley Retainer, Palatal Expander, Spacer, Herbst, Nance HoldingArch by Shenzhen Minghao Dentures Co., Ltd. — Class N — FDA UDI — listed in FDA…

Similar devices

Also classified as Orthodontic retainer.

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

Sources (1)

  • FDA UDI 116a7fdd-f13b-42be-8604-f4d93126a520 32 fields · synced May 30, 2026