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Creatures of the Sea

FDA UDI

Class I (US FDA UDI)

by Ortho Technology, Inc.

Identity

Trade Name
Creatures of the Sea FDA UDI
Generic Name
Orthodontic inter-arch elastic band FDA UDI
Device Name
Elastics Amber Medium 3/16" Sea Otter 50 pks of 100 FDA UDI
Model / Reference
500-202 FDA UDI
Description
Elastics Amber Medium 3/16" Sea Otter 50 pks of 100 FDA UDI

Identifiers

Primary DI / UDI-DI
00190730007070 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic inter-arch elastic band

Creatures of the Sea by Ortho Technology, Inc. — 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

Sources (1)

  • FDA UDI 9e0aadd3-24cc-4777-8e6c-64bac93a593f 33 fields · synced May 31, 2026