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PDS Plates

FDA UDI

Class II (US FDA UDI)

by Ethicon Inc.

Identity

Trade Name
PDS Plates FDA UDI
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI
Device Name
PDS FLEX PLATE 0.25X40X50MM NASAL IMPLANT FDA UDI
Model / Reference
ZFP5 FDA UDI
Description
PDS FLEX PLATE 0.25X40X50MM NASAL IMPLANT FDA UDI

Identifiers

Catalog Number
ZFP5 FDA UDI
Primary DI / UDI-DI
10705031132511 FDA UDI
510(k) Number
K092590 FDA UDI
FDA Product Code
NHB FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3620 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: Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable

PDS Plates by Ethicon Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ethicon Inc.

Sources (1)

  • FDA UDI c33ac93e-8aff-489c-b8e0-e6f7ab16bc29 36 fields · synced Jun 8, 2026