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Surfix 285332SND

by Newdeal Sas

Surfix 285332SND is a Class II device made by Newdeal Sas, cleared under FDA 510(k) K093914 on 14 Apr 2011 (5 earlier submissions) and listed in FDA GUDID since 9 Oct 2017 (UDI-DI 10381780049098), active as of 23 Oct 2026. 9 FDA recalls are linked to it.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10381780049098 UDI-DI Date9 Oct 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK093914 Date14 Apr 2011DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K093914 decided 14 Apr 2011 Active· +5 more in the status table
  • FDA GUDID UDI-DI 10381780049098 listed 9 Oct 2017 Listed

Recalls

10 recalls · 1 ongoing · FDA

    • Ongoing Z-0548-2022 FDA Class II initiated 4 Jan 2022

    The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw

  • 5 recalls, same reason

    • Terminated Z-2444-2018 FDA Class II initiated 22 May 2018
    • Terminated Z-2446-2018 FDA Class II initiated 22 May 2018
    • Terminated Z-2443-2018 FDA Class II initiated 22 May 2018
    • Terminated Z-2447-2018 FDA Class II initiated 22 May 2018
    • Terminated Z-2445-2018 FDA Class II initiated 22 May 2018

    Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.

    • Terminated Z-1697-2014 FDA Class II initiated 28 Mar 2014 on shared 510(k) K073375

    New Deal has identified through a complaint report that some 3.5 mm Diameter x 22 mm Length Surfix screws in Lot no. F626 (Catalogue No. 285322S) have been packaged and labeled as 3.5mm Diameter x 30 mm Length Surfix screws (Catalogue No. 285330S).

    • Terminated Z-2123-2012 FDA Class II initiated 9 Feb 2012

    Incorrect technique applied may cause potential rupture of the tibialis anterior tendon during surgery.

    • Terminated Z-0955-2011 FDA Unclassified (pre-2012) initiated 18 Nov 2010

    Integra LifeSciences Corporation has decided to initiate a voluntary recall of the Uni-Comp Kits due to inaccurate information relative to the recommended sterilization parameters described in the products Instructions for Use (IFU). The sterilization parameters noted in the Uni-Comp IFU were incorrect. It is noted that the sterilization recommendations in the UNI-Comp IFU in which the Exposure

    • Terminated Z-0307-2009 FDA Unclassified (pre-2012) initiated 30 Sep 2008

    Reports of the Uni-CP Compression Forceps breaking during the Compression of the Uni-CP plate

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

17 dated events

  1. Cleared FDA 510(k) K093914
  2. Recall initiated FDA recalls Z-2123-2012
  3. Recall initiated FDA recalls Z-1697-2014
  4. Listed FDA GUDID 10381780049098
  5. Recall initiated FDA recalls Z-2444-2018
  6. Recall initiated FDA recalls Z-2446-2018
  7. Recall initiated FDA recalls Z-2443-2018
  8. Recall initiated FDA recalls Z-2447-2018
  9. Recall initiated FDA recalls Z-2445-2018
  10. Recall initiated FDA recalls Z-0548-2022

7 earlier events are in the sections above.

Coverage

1 jurisdiction

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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Surfix
Generic name
Orthopaedic bone screw, non-bioabsorbable, sterile
Model / Ref / Catalog
285332SND
Primary DI / UDI-DI
10381780049098
510(k) Number
FDA product code
HRS
GMDN term
Orthopaedic bone screw, non-bioabsorbable, sterile
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Cleared under the same submission (K063820)

and 8 more cleared under K063820

Cleared under the same submission (K070241)

and 8 more cleared under K070241

Similar devices in this category

Other devices filed under Orthopaedic bone screw, non-bioabsorbable, sterile.

Other devices from Newdeal Sas

See all devices from Newdeal Sas →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)