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Speed SE-2520

by Biomedical Enterprises, Inc.

Speed SE-2520 is a Class II device made by Biomedical Enterprises, Inc., listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00810633020234), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810633020234 UDI-DI Date24 Oct 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  • Withdrawn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
Speed
Generic name
Orthopaedic bone staple, non-adjustable
Model / reference
SE-2520
Primary DI / UDI-DI
00810633020234
FDA product code
JDR
GMDN term
Orthopaedic bone staple, non-adjustable
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Width — 25 Millimeter
Length — 20 Millimeter

Related devices

Category: Orthopaedic bone staple, non-adjustable

Similar devices in this category

Other devices filed under Orthopaedic bone staple, non-adjustable.

Other devices from Biomedical Enterprises, Inc.

See all devices from Biomedical Enterprises, Inc. →

Properties

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