Medline

Mundelein, IL, US

Medline appears in FDA device records in Mundelein, IL. FDA records list 11 510(k) clearances between 1992-04-29 and 2012-02-08, no PMA records and no registered establishments. As of 2026-09-10, FDA records show no recalls for this company.

510(k) clearances: 11
PMA records: 0
Recall records: 0
Registered establishments: 0

510(k) clearance history

FDA records hold 11 510(k) clearances for Medline between 1992 and 2012. The busiest year on record is 1995, with 2. The most recent is 2012, with 1.

Clearances by year, as a table

510(k) clearance decisions for Medline, by decision year
Year	Clearances
1992	1
1994	1
1995	2
1996	2
1997	1
1999	1
2001	1
2005	1
2012	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K120156	PUREIMAGE ULTRASOUND TRANSMISSION GEL	ITX	Substantially Equivalent	2012-02-08
K051378	POWDER-FREE BLUE NITRILE EXAMINATION GLOVES (TESTED FOR USE WITH CHEMOTHERAPY DRUGS)	LZA	Substantially Equivalent	2005-08-03
K010825	MEDLINE STERISET STERILIZATION CONTAINER	FRG	Substantially Equivalent	2001-05-08
K990463	MEDLINE EXCEL WHEELCHAIRS	IOR	Substantially Equivalent	1999-03-15
K970282	MEDLINE CIRCUMCISION TRAY	HFX	Substantially Equivalent	1997-03-06
K963504	MEDLINE OPEN END FINGER CONTROL MITT	FMQ	Substantially Equivalent	1996-10-29
K963452	MEDLINE ZIPPER SLEEVED VEST	FMQ	Substantially Equivalent	1996-10-18
K951736	LOCK-UP	FMI	Substantially Equivalent	1995-07-05
K932033	LAPAROSCOPIC SURGERY INSTRUMENTS	GCJ	Substantially Equivalent	1995-06-19
K932060	MARTIN COLD LIGHT FOUNTAIN	GCJ	Substantially Equivalent	1994-03-30
K915502	MEDLINE, GORE-TEX BARRIER, SURGICAL GOWNS & DRAPES	FYA	Substantially Equivalent	1992-04-29

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