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Dyonics / Full Radius

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS / FULL RADIUS FDA UDI
Generic Name
Arthroscopic shaver system blade, single-use FDA UDI
Device Name
FULL RADIUS MINI IRRIGATING FDA UDI
Model / Reference
7205688 FDA UDI
Description
FULL RADIUS MINI IRRIGATING FDA UDI

Identifiers

Catalog Number
7205688 FDA UDI
Primary DI / UDI-DI
00885554009132 FDA UDI
510(k) Number
K970511 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Arthroscopic shaver system blade, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

Category: Arthroscopic shaver system blade, single-use

Dyonics / Full Radius by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system blade, single-use.

Cleared under the same submission

K970511 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 2be02f91-af0d-4f40-8902-093e7a779138 36 fields · synced Jun 8, 2026