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Resorb Xg, Sterile

FDA UDI

Class II (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
RESORB XG, STERILE FDA UDI
Generic Name
Craniofacial fixation plate, bioabsorbable FDA UDI
Device Name
MESH, SMALL GRID, PLLA-PGA FDA UDI
Model / Reference
52-803-50-04 FDA UDI
Description
MESH, SMALL GRID, PLLA-PGA FDA UDI

Identifiers

Primary DI / UDI-DI
00888118001313 FDA UDI
FDA Product Code
GWO FDA UDI
HBW FDA UDI
GMDN Term
Craniofacial fixation plate, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5320 FDA UDI
882.5360 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: Craniofacial fixation plate, bioabsorbable

Resorb Xg, Sterile by KLS-Martin L.P. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial fixation plate, bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI f0f6ce7b-b4da-4ed7-bd22-f2b44f47acce 35 fields · synced May 30, 2026