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Pro-Elast

FDA UDI

Class I (US FDA UDI)

by Ortho Pro Dent LLC

Identity

Trade Name
PRO-ELAST FDA UDI
Generic Name
Orthodontic inter-arch elastic band FDA UDI
Device Name
Latex elastics Extra-Heavy 6.0 oz 3/16" 50 pks of 100 FDA UDI
Model / Reference
EL-0616 FDA UDI
Description
Latex elastics Extra-Heavy 6.0 oz 3/16" 50 pks of 100 FDA UDI

Identifiers

Primary DI / UDI-DI
00810152822036 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic inter-arch elastic 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic inter-arch elastic band

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

Similar devices

Also classified as Orthodontic inter-arch elastic 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 a01e754b-e6d9-4b2d-aec6-0c4f8ea061fe 34 fields · synced Jun 8, 2026