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Dyonics / Synovator 72201077

by Smith & Nephew, Inc.

Dyonics / Synovator 72201077 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 28 Sep 2015 (UDI-DI 00885554014587), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885554014587 UDI-DI Date28 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Dyonics / Synovator
Generic name
Arthroscopic shaver system blade, single-use
Model / Ref / Catalog
72201077
Primary DI / UDI-DI
00885554014587
FDA product code
HAB
GMDN term
Arthroscopic shaver system blade, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Arthroscopic shaver system blade, single-use

Similar devices in this category

Other devices filed under Arthroscopic shaver system blade, single-use.

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)