← Back to catalogue

In2Bones

FDA UDI

Class I (US FDA UDI)

by In2Bones, USA

Identity

Trade Name
In2Bones FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Torque-Limiting Ratchet Handle AO QC, 11 in-lbs, Non-Sterile FDA UDI
Model / Reference
P04 N0441 FDA UDI
Description
Torque-Limiting Ratchet Handle AO QC, 11 in-lbs, Non-Sterile FDA UDI

Identifiers

Catalog Number
P04 N0441 FDA UDI
Primary DI / UDI-DI
00810021867090 FDA UDI
510(k) Number
K163293 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Surgical instrument handle, non-torque-limiting

In2Bones by In2Bones, USA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
In2Bones, USA

Sources (1)

  • FDA UDI f4d15131-2a14-417a-a092-5f943395d92d 36 fields · synced May 30, 2026