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Genesis

FDA UDI

Class I (US FDA UDI)

by Keystone Dental Inc.

Identity

Trade Name
Genesis FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Implant Driver FDA UDI
Model / Reference
G21292 FDA UDI
Description
Implant Driver FDA UDI

Identifiers

Primary DI / UDI-DI
D768G212920 FDA UDI
510(k) Number
K101545 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical screwdriver, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical screwdriver, reusable

Genesis by Keystone Dental Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7484519e-ee13-42a8-8035-c8d435de189f 35 fields · synced May 30, 2026