Sr Instruments Inc

Tonawanda, NY, US

SR INSTRUMENTS, INC. appears in FDA device records in Tonawanda, NY. FDA records list 2 510(k) clearances, no PMA records and one registered establishment. As of 2026-09-10, FDA records show one recall for this company, and at least one establishment registration is current.

510(k) clearances: 2
PMA records: 0
Recall records: 1
Registered establishments: 1

510(k) clearance history

FDA records hold 2 510(k) clearances for Sr Instruments Inc in 1977.

Clearances by year, as a table

510(k) clearance decisions for Sr Instruments Inc, by decision year
Year	Clearances
1977	2

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K770848	DAILY-WEIGHT	FRI	Substantially Equivalent	1977-06-08
K770847	PORTA-SCALE	FRI	Substantially Equivalent	1977-06-08

Registered establishments

FDA registered establishments for Sr Instruments Inc, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
1317256	1317256	SR INSTRUMENTS, INC.	600 YOUNG ST., Tonawanda, NY 14150 US	2026	FQA FRI FRW FTY INF

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
Recall	Product	Reason	Classification	Initiated	Status
Z-1128-2013	SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare Patient Lifters. Model# FG3105 Patient Scales. Product Usage: The FG3105 Scale is designed for Joerns Healthcare for use in portable patient weighing systems. The scale is designed to be connected between the patient hoist mechanism and patient sling apparatus. The scale is not intended to be used for patient transport.	SR Instruments Inc. is implementing a field correction for the Joerns Healthcare Patient Lifts after they received two incident reports regarding two field failures of a tensile type load cell involving the FG3105 Patient Scale. The failures resulted in patient falls.	Class II	2012-12-13	Terminated

Verification record

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