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SecureVac™ Immobilization System SVRT-7915

by Bionix, LLC

SecureVac Immobilization System SVRT-7915 is a radiological whole-body positioner (FDA Class II; FDA product code IYE, Accelerator, linear, medical) made by Bionix, LLC, cleared under FDA 510(k) K040773 on 9 Apr 2004 and listed in FDA GUDID since 9 Jul 2022 (UDI-DI 00714646000293), active as of 22 Oct 2026.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K040773

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00714646000293 UDI-DI Date9 Jul 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK040773 Date9 Apr 2004DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K040773 decided 9 Apr 2004 Active
  • FDA GUDID UDI-DI 00714646000293 listed 9 Jul 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K040773
  2. Listed FDA GUDID 00714646000293

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
SecureVac™ Immobilization System
Generic name
Radiological whole-body positioner
Model / Ref / Catalog
SVRT-7915
Primary DI / UDI-DI
00714646000293
510(k) Number
FDA product code
IYE
GMDN term
Radiological whole-body positioner
Device class
Class II
Regulation number
892.5050
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

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Other devices filed under Radiological whole-body positioner.

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)