← Back to catalogue

Accelus Navigated Reusable Instruments

FDA UDI

Class II (US FDA UDI)

by Integrity Implants Inc.

Identity

Trade Name
Accelus Navigated Reusable Instruments FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Nav Modular Shank Driver - SM Ball FDA UDI
Model / Reference
ASY-00730 FDA UDI
Description
Nav Modular Shank Driver - SM Ball FDA UDI

Identifiers

Catalog Number
ASY-00730 FDA UDI
Primary DI / UDI-DI
00810045534473 FDA UDI
510(k) Number
K212088 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

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

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 screwdriver, reusable

Accelus Navigated Reusable Instruments by Integrity Implants Inc. — Class II — 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

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

Manufacturer

Sources (1)

  • FDA UDI c9c0d8f2-fdc3-45e8-9df7-55a7d7decdb2 36 fields · synced Jun 6, 2026