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Single Arm Trapeze Assembly ASM100105

by Kreg Medical, Inc.

Single Arm Trapeze Assembly ASM100105 is a Class I device made by Kreg Medical, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 00850520008006), 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 Number00850520008006 UDI-DI Date21 Sep 2018ListedStatusListed 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  • Withdrawn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
Single Arm Trapeze Assembly
Generic name
Bed traction frame
Model / reference
ASM100105
Primary DI / UDI-DI
00850520008006
FDA product code
ILZ
GMDN term
Bed traction frame
Device class
Class I
Regulation number
890.5925
GUDID distribution status
In Commercial Distribution

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Category: Bed traction frameTrapeze bar exerciser

Other devices from Kreg Medical, Inc.

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Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)