← Back to catalogue

Iconacy i-Hip

FDA UDI

Class II (US FDA UDI)

by Iconacy Orthopedic Implants, LLC

Identity

Trade Name
Iconacy i-Hip FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
BONE SCREW, 6.5MM DIAMETER, 40MM LENGTH FDA UDI
Model / Reference
01-10901-040-00 FDA UDI
Description
BONE SCREW, 6.5MM DIAMETER, 40MM LENGTH FDA UDI

Identifiers

Catalog Number
01-10901-040-00 FDA UDI
Primary DI / UDI-DI
M914011090104000 FDA UDI
510(k) Number
K121034 FDA UDI
FDA Product Code
LWJ FDA UDI
LPH FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
888.3358 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 40 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Iconacy i-Hip by Iconacy Orthopedic Implants, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

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 33985be2-50ba-43c1-b6dd-3860539cdedd 37 fields · synced Jun 1, 2026