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Sinton Medical Products 600102-20

by Shenzhen Boon Medical Supply Co., Ltd.

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 Number06938327902926 UDI-DI Date19 Aug 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  • Withdrawn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
Sinton Medical Products
Generic Name
Radiographic procedure tubing
Model / Ref / Catalog
600102-20, HT-LY2502
Primary DI / UDI-DI
06938327902926
510(k) Number
FDA Product Code
DXT
GMDN Term
Radiographic procedure tubing
Device Class
Class II
Regulation Number
870.1650
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K241109)

Show all (12)

Other devices from Shenzhen Boon Medical Supply Co., Ltd.

See all devices from Shenzhen Boon Medical Supply Co., Ltd. →

Properties

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

Other properties (8)

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