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Blepharoplasty kit SBK-01

by Soniquence, LLC

Blepharoplasty kit SBK-01 is a device made by Soniquence, LLC, listed in FDA GUDID since 11 Apr 2022 (UDI-DI 00810026180248), 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 Number00810026180248 UDI-DI Date11 Apr 2022ListedStatusListed 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  • Withdrawn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
Blepharoplasty kit
Generic name
Electrical-only medical device connection cable, single-use
Model / Ref / Catalog
SBK-01
Primary DI / UDI-DI
00810026180248
GMDN term
Electrical-only medical device connection cable, single-use
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices in this category

Other devices filed under Electrosurgical handpiece, single-use.

Other devices from Soniquence, LLC

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)