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Ortho Pro

FDA UDI

Class I (US FDA UDI)

by Ortho Pro Dent LLC

Identity

Trade Name
Ortho Pro FDA UDI
Generic Name
Orthodontic metal band FDA UDI
Device Name
lingual sheath Bondable Without Hook or Indent 10 pcs/pk FDA UDI
Model / Reference
CSS-LS-200 FDA UDI
Description
lingual sheath Bondable Without Hook or Indent 10 pcs/pk FDA UDI

Identifiers

Primary DI / UDI-DI
00810152826300 FDA UDI
FDA Product Code
ECM FDA UDI
GMDN Term
Orthodontic metal band FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic metal band

Ortho Pro by Ortho Pro Dent LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic metal band.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortho Pro Dent LLC

Sources (1)

  • FDA UDI 32a6c72b-4ac7-484a-84fe-2b7fc9124756 35 fields · synced May 30, 2026