← Back to catalogue

Sherlock

FDA UDI

Class II (US FDA UDI)

by Open Implants

Identity

Trade Name
Sherlock FDA UDI
Generic Name
Dental prosthesis/implant abutment screw FDA UDI
Device Name
Sherlock Abutment Screw, Nobel Replace Select 3.5 NP Compatible FDA UDI
Model / Reference
3756 FDA UDI
Description
Sherlock Abutment Screw, Nobel Replace Select 3.5 NP Compatible FDA UDI

Identifiers

Catalog Number
3756 FDA UDI
Primary DI / UDI-DI
D86337560 FDA UDI
510(k) Number
K961384 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental prosthesis/implant abutment screw

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

Similar devices

Also classified as Dental prosthesis/implant abutment screw.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Open Implants

Sources (1)

  • FDA UDI cbade037-90ec-481a-a9ec-05af7c1a2686 35 fields · synced May 30, 2026