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Peri-Loc

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Peri-Loc FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
PERI-LOC 4.5MM TITANIUM LATERAL DISTAL FEMUR PLATE 8 HOLE RIGHT 193MM FDA UDI
Model / Reference
71860108 FDA UDI
Description
PERI-LOC 4.5MM TITANIUM LATERAL DISTAL FEMUR PLATE 8 HOLE RIGHT 193MM FDA UDI

Identifiers

Catalog Number
71860108 FDA UDI
Primary DI / UDI-DI
03596010640178 FDA UDI
510(k) Number
K083032 FDA UDI
K210837 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Orthopaedic fixation plate, non-bioabsorbable

Peri-Loc by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 98d3cbd3-01aa-4498-8f0c-d2bc5c79d0e3 36 fields · synced Jun 8, 2026