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Sherlock

FDA UDI

Class I (US FDA UDI)

by Open Implants

Identity

Trade Name
Sherlock FDA UDI
Generic Name
Dental implant analog FDA UDI
Device Name
Sherlock Implant Analog, Zimmer Tapered Screw Vent 3.5 -- Bulk Quantity 25; Green FDA UDI
Model / Reference
3611 FDA UDI
Description
Sherlock Implant Analog, Zimmer Tapered Screw Vent 3.5 -- Bulk Quantity 25; Green FDA UDI

Identifiers

Primary DI / UDI-DI
D86336112 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant analog 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

No

FDA UDI

Category: Dental implant analog

Sherlock by Open Implants — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant analog.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Open Implants

Sources (1)

  • FDA UDI ace756d0-d2d7-4136-989c-61bce8afdf48 33 fields · synced May 30, 2026