Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008252121

FEI Number

3008252121

Entity Name

OD-OS GMBH

City/State/Country

Teltow Brandenburg, DE

Establishment Address

Warthestr. 21, Teltow Brandenburg 14513, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

OD-OS GmbH (Owner Number: 10031430)

Owner / Operator Contact Address

Warthestr. 21, Teltow, DE-BB 14513, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K251772

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQF	Laser, Ophthalmic	Ophthalmic	Class 2	886.4390	2026-01-13

Official Correspondent

No official correspondent registered.

US Agent Details

Trey Pleasants Business: OD-OS, Inc Email: od-os.usagent@od-os.com Phone: (949) 4157256

Related Public Records

Same Entity

OD-OS GmbH

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K834060	F. & F. Koenigkramer	RELIANCE OPHTHALMIC SLIT LAMP R-083	1984-02-04

Similar Registrations

Registration Number	Establishment Name	Location
3009462521	Oncore Manufacturing, LLC dba NEOTech	Fremont, CA, US
2028159	Alcon Research, LLC	IRVINE, CA, US
2247224	Beaver-Visitec International, Inc	Little Silver, NJ, US
3007851054	Avedro, A Glaukos Company	Burlington, MA, US
2031962	STALLION MEDICAL, INC.	SAN DIEGO, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008252121. Last updated year: 2026. Please use registration number 3008252121 when referencing this establishment in official correspondence.