Sonotech, Inc.

Bellingham, WA, US

Sonotech, Inc. appears in FDA device records in Bellingham, WA. FDA records list 14 510(k) clearances between 1995-10-17 and 2004-11-05, no PMA records and no registered establishments. As of 2026-09-10, FDA records show no recalls for this company.

510(k) clearances: 14
PMA records: 0
Recall records: 0
Registered establishments: 0

510(k) clearance history

FDA records hold 14 510(k) clearances for Sonotech, Inc. between 1995 and 2004. The busiest year on record is 1999, with 3. The most recent is 2004, with 2.

Clearances by year, as a table

510(k) clearance decisions for Sonotech, Inc., by decision year
Year	Clearances
1995	1
1996	2
1997	1
1998	1
1999	3
2001	1
2002	1
2003	2
2004	2

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K042619	ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT	MUI	Substantially Equivalent	2004-11-05
K033178	ULTRABIO	MUI	Substantially Equivalent	2004-08-04
K031222	SCANLUBE	MUI	Substantially Equivalent	2003-07-23
K031894	SCANTEC PAD	MUI	Substantially Equivalent	2003-07-18
K013701	ENDO-GLIDE	GCJ	Substantially Equivalent	2002-02-04
K013170	SCANTAC MEMBRANE OR SCANTAC STRIP	ITX	Substantially Equivalent	2001-11-13
K984562	VIVOSONIC	ITX	Substantially Equivalent	1999-06-08
K983691	SCANFLEX SOLID COUPLANT MEMBRANE	ITX	Substantially Equivalent	1999-05-05
K983985	HYBRISONIC SHEATH	ITX	Substantially Equivalent	1999-02-25
K981028	ULTRA IMAGE AND ULTRA SCAN	ITX	Substantially Equivalent	1998-08-21
K964658	OASIS	ITX	Substantially Equivalent	1997-02-14
K962093	ULTRAMIX	ITX	Substantially Equivalent	1996-12-23
K961692	SONOSCAN	ITX	Substantially Equivalent	1996-08-22
K953468	SONOGEL	IYO	Substantially Equivalent	1995-10-17

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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What MDM checks, and what it does not

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain