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OCO-LOK Impression Pickup

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name
OCO-LOK Impression Pickup FDA UDI
Generic Name
Dental implant abutment impression cap FDA UDI
Device Name
OCO-LOK Impression Pickup (2 PK) FDA UDI
Model / Reference
OCO-LOK Impression Pickup FDA UDI
Description
OCO-LOK Impression Pickup (2 PK) FDA UDI

Identifiers

Catalog Number
LOK PU-2 FDA UDI
Primary DI / UDI-DI
D785LOKPU20 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment impression cap 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant abutment impression cap

OCO-LOK Impression Pickup by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant abutment impression cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oco Biomedical

Sources (1)

  • FDA UDI 59a8968c-8671-433b-b7c6-9c49873d9186 34 fields · synced May 30, 2026