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iTotal® Hip Replacement System

FDA UDI

Class II (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
iTotal® Hip Replacement System FDA UDI
Generic Name
Acetabular orthopaedic reamer FDA UDI
Device Name
HIP-REAMER STAGE 1-56MM FDA UDI
Model / Reference
HAR000S15601 FDA UDI
Description
HIP-REAMER STAGE 1-56MM FDA UDI

Identifiers

Catalog Number
HAR000S156 FDA UDI
Primary DI / UDI-DI
M572HAR000S156011 FDA UDI
510(k) Number
K162719 FDA UDI
FDA Product Code
OQG FDA UDI
MEH FDA UDI
LZO FDA UDI
LPH FDA UDI
GMDN Term
Acetabular orthopaedic reamer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acetabular orthopaedic reamer

iTotal® Hip Replacement System by Conformis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI 1bc38474-d700-4913-abd5-124d62415691 37 fields · synced May 31, 2026