Data / Medical devices / United States / Grace Manufacturing Inc

Grace Manufacturing Inc: FDA-registered device maker in Russellville, AR, United States, 3 510(k) clearances

Name: Grace Manufacturing Inc FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Grace Manufacturing Inc is registered with the FDA (registration 1651252) in Russellville, AR, United States. It lists 17 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 1, 1994. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 1651252
FEI number: 3002770040
Address: 614 SR 247, Russellville, AR, United States, 72802
Owner or operator: Grace Manufacturing Inc (10042478)
Roles: Contract manufacturer, Manufacturer
First device listed: November 30, 2012
Registered through: 2026
Brand names listed: Active Cord BSC, Reusable Monopolar Active Cord

Devices it lists

Device	Product code	Class	Role	Source
Blade, Saw, General & Plastic Surgery, Surgical	GFA	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Bougie, Urological	FAX	1	Manufacturer	accessdata.fda.gov
Cannula And Trocar, Suprapubic, Non-Disposable	FBM	1	Manufacturer	accessdata.fda.gov
Clamp, Penile	FHA	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)	HIN	2	Manufacturer	accessdata.fda.gov
Cord, Electric For Transurethral Surgical Instrument	FBJ	2	Manufacturer	accessdata.fda.gov
Dislodger, Stone, Basket, Ureteral, Metal	FFL	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Electrocautery, Gynecologic (And Accessories)	HGI	2	Manufacturer	accessdata.fda.gov
Electrode, Electrosurgical, Active, Urological	FAS	2	Manufacturer	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Endoscopic Tissue Approximation Device	OCW	2	Contract manufacturer	accessdata.fda.gov
Reamer	HTO	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Retractor, Non-Self-Retaining	FGN	1	Manufacturer	accessdata.fda.gov
Sound, Urethral, Metal Or Plastic	FBX	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Stylet For Catheter, Gastro-Urology	EZB	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Surgical Instruments, G-U, Manual (And Accessories)	KOA	1	Manufacturer	accessdata.fda.gov
Unit, Electrosurgical, Endoscopic (With Or Without Accessories)	KNS	2	Contract 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
April 1, 1994	K933175	GREENWALD CONTROL TIP URETEROSCOPIC ELECTRODE	FAS	Substantially Equivalent	Greenwald Surgical Co., Inc.	accessdata.fda.gov
April 1, 1994	K933174	GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE	FAS	Substantially Equivalent	Greenwald Surgical Co., Inc.	accessdata.fda.gov
April 1, 1994	K933173	GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE	FAS	Substantially Equivalent	Greenwald Surgical Co., Inc.	accessdata.fda.gov

Compare with other makers

Updated April 1, 1994. 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.