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532.015

by Synthes GmbH

532.015 (532015) is a reaming power tool attachment (FDA Class I; FDA product code HWE, Instrument, Surgical, Orthopedic, Ac-Powered Motor and Accessory/Attachment) made by Synthes GmbH, listed in FDA GUDID since 31 Dec 2016 (UDI-DI 10886982240477), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10886982240477 UDI-DI Date31 Dec 2016ListedStatusListed 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  • Withdrawn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

Generic name
Reaming power tool attachment
Model / Ref / Catalog
532.015, 532015
Primary DI / UDI-DI
10886982240477
FDA product code
HWE
GMDN term
Reaming power tool attachment
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Reaming power tool attachment

Similar devices

Other devices filed under FDA product code HWE (INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT).

Other devices from Synthes GmbH

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  • 68.134.011

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  • Volt 68.134.111

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See all devices from Synthes GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)