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H-MAX S Lateralizing

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
H-MAX S Lateralizing FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
H-MAX S Lateralizing Uncemented stems (Ti6Al4V + HA) n.14 FDA UDI
Model / Reference
Uncemented Stem FDA UDI
Description
H-MAX S Lateralizing Uncemented stems (Ti6Al4V + HA) n.14 FDA UDI

Identifiers

Catalog Number
4251.20.140 FDA UDI
Primary DI / UDI-DI
08033390051743 FDA UDI
510(k) Number
K112091 FDA UDI
K150855 FDA UDI
K160011 FDA UDI
FDA Product Code
MEH FDA UDI
JDI FDA UDI
KWY FDA UDI
LPH FDA UDI
GMDN Term
Coated femoral stem prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3350 FDA UDI
888.3390 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

Yes

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

Category: Coated femoral stem prosthesis, modular

H-MAX S Lateralizing by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 05b8123f-b241-48ae-85c7-ef6656ca0355 36 fields · synced Jun 8, 2026