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Retaining Ring With O-Ring

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name
RETAINING RING WITH O-RING FDA UDI
Generic Name
Denture clasp, polymer, preformed FDA UDI
Device Name
003 RETAINING RING WITH O-RING INSERTED FDA UDI
Model / Reference
003 RETAINING RING WITH O-RING INSERTED FDA UDI
Description
003 RETAINING RING WITH O-RING INSERTED FDA UDI

Identifiers

Catalog Number
003 RR W/O-RING FDA UDI
Primary DI / UDI-DI
D785003RRWO0 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Denture clasp, polymer, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Denture clasp, polymer, preformed

Retaining Ring With O-Ring by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture clasp, polymer, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oco Biomedical

Sources (1)

  • FDA UDI 1b7499f7-cc4b-4c5a-819b-c9a6ac319a94 34 fields · synced May 30, 2026