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Implant-One

FDA UDI

Class I (US FDA UDI)

by Implant Logistics, Inc.

Identity

Trade Name
Implant-One FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Interchangeable Driver Assembly, Radiographic Marker (RAM) Driver FDA UDI
Model / Reference
IDS-0000-00 FDA UDI
Description
Interchangeable Driver Assembly, Radiographic Marker (RAM) Driver FDA UDI

Identifiers

Primary DI / UDI-DI
D762IDS0000000 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

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: Surgical instrument handle, non-torque-limiting

Implant-One by Implant Logistics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7acb0a85-1396-4cf7-bd8b-530aa25e8780 34 fields · synced May 30, 2026