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ActivaScrew™ B-ACC-3528

by Bioretec Oy

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06438394020054 UDI-DI Date16 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ActivaScrew™
Generic Name
Bioabsorbable orthopaedic bone screw
Model / Ref / Catalog
B-ACC-3528
Primary DI / UDI-DI
06438394020054
510(k) Number
FDA Product Code
HWC
GMDN Term
Bioabsorbable orthopaedic bone screw
Device Class
Class II
Regulation Number
888.3040
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Length — 28 Millimeter
Width — 3.5 Millimeter

Related devices

Cleared under the same submission (K261057)

Show all (12)

Other devices from Bioretec Oy

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No