Advanced Back Technologies

Syosset, NY, US

Advanced Back Technologies appears in FDA device records in Syosset, NY. FDA records list 2 510(k) clearances between 1998-05-11 and 2004-07-23, no PMA records and no registered establishments. As of 2026-09-10, FDA records show 2 recalls for this company.

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

510(k) clearance history

FDA records hold 2 510(k) clearances for Advanced Back Technologies between 1998 and 2004. The busiest year on record is 1998, with 1. The most recent is 2004, with 1.

Clearances by year, as a table

510(k) clearance decisions for Advanced Back Technologies, by decision year
Year	Clearances
1998	1
2004	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K031996	EXTENTRAC ELITE	ITH	Substantially Equivalent	2004-07-23
K980021	EXTENTRAC	JFB	Substantially Equivalent	1998-05-11

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

Device recall records naming this company, most recent first
Recall	Product	Reason	Classification	Initiated	Status
Z-1718-2015	Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction)	Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs	Class II	2015-05-13	Terminated
Z-1717-2015	Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)	Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs	Class II	2015-05-13	Terminated

Verification record

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