Data / Medical devices / Germany / Bausch & Lomb Incorporated

Bausch & Lomb Incorporated: FDA-registered device maker in Eppelheim Baden-Wurttemberg, Germany, 2 510(k) clearances

Name: Bausch & Lomb Incorporated FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Bausch & Lomb Incorporated is registered with the FDA (registration 3029990829) in Eppelheim Baden-Wurttemberg, Germany. It lists 20 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 12, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3029990829
Address: Lilienthalstr. 16, 18, Eppelheim Baden-Wurttemberg, Germany, 69214
Owner or operator: Bausch & Lomb Incorporated (9913003)
Roles: Manufacturer
First device listed: January 1, 1993
Registered through: 2026

Devices it lists

Device	Product code	Class	Role	Source
Caliper, Ophthalmic	HOE	1	Manufacturer	accessdata.fda.gov
Cannula, Ophthalmic	HMX	1	Manufacturer	accessdata.fda.gov
Curette, Ophthalmic	HNZ	1	Manufacturer	accessdata.fda.gov
Depressor, Orbital	HNX	1	Manufacturer	accessdata.fda.gov
Eye Tray	OJK	2	Manufacturer	accessdata.fda.gov
Forceps, Ophthalmic	HNR	1	Manufacturer	accessdata.fda.gov
Hook, Ophthalmic	HNQ	1	Manufacturer	accessdata.fda.gov
Knife, Ophthalmic	HNN	1	Manufacturer	accessdata.fda.gov
Needle, Ophthalmic Suturing	HNM	1	Manufacturer	accessdata.fda.gov
Probe, Lachrymal	HNL	1	Manufacturer	accessdata.fda.gov
Probe, Radiofrequency Lesion	GXI	2	Manufacturer	accessdata.fda.gov
Retractor, Ophthalmic	HNI	1	Manufacturer	accessdata.fda.gov
Ring, Ophthalmic (Flieringa)	HNH	1	Manufacturer	accessdata.fda.gov
Rongeur, Lachrymal Sac	HNG	1	Manufacturer	accessdata.fda.gov
Scissors, Ophthalmic	HNF	1	Manufacturer	accessdata.fda.gov
Spatula, Ophthalmic	HND	1	Manufacturer	accessdata.fda.gov
Specula, Ophthalmic	HNC	1	Manufacturer	accessdata.fda.gov
Spoon, Ophthalmic	HNB	1	Manufacturer	accessdata.fda.gov
Trabeculotome	HMZ	1	Manufacturer	accessdata.fda.gov
Unit, Phacofragmentation	HQC	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 12, 2008	K073023	STERILS SINGLE-USE I/A HANDPIECES	HQC	Substantially Equivalent	Bausch & Lomb, Inc.	accessdata.fda.gov
August 17, 1988	K882802	STORZ DISPOSABLE BIPOLAR PENCILS	GXI	Substantially Equivalent	Storz Instrument Co.	accessdata.fda.gov

Compare with other makers

Updated March 12, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.