Bruno Independent Living Aids, Inc.: FDA filings under this applicant name

FDA lists 12 510(k) clearances under the applicant name “Bruno Independent Living Aids, Inc.” (first 1992, latest 2012), across 5 product codes in 1 review panel. Median 510(k) review time under this name: 26 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
2012184
20130—
20140—
20150—
20160—
20170—
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
ILKTransport, Patient, Powered77
ITIWheelchair, Powered22
INGElevator, Wheelchair, Portable11
INIVehicle, Motorized 3-Wheeled11
IORWheelchair, Mechanical11

Review panels

Most recent Bruno Independent Living Aids, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K113308BRUNO ELAN STAIRWAY ELEVATORILK2012-02-0184
K061514BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100ING2006-07-1342
K033829BRUNO ELECTRA-RIDE III STAIRWAY ELEVATOR SYSTEM, MODEL CRE-2100ILK2003-12-2920
K033752BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540ILK2003-12-1211
K033438BRUNO ELECTRA-RIDE ELITE, MODEL SRE-2000ILK2003-11-2023
K022509BRUNO ELECTRA-RIDE, MODEL SRE-2700ILK2002-08-1314
K011227REGAL MOTOTRIZED 3 WHEELED VEHICLEITI2001-05-1118
K002205CARONYIOR2000-08-1020
K991954THE BRUNO POWERBASE, MODEL PSB-2200ITI1999-11-02145
K970927BRUNO ELECTRA-RIDE III STAIRWAY ELEVATOR SYSTEMILK1997-08-26166

2 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Bruno Independent Living Aids, Inc..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Bruno Independent Living Aids, Inc.?

FDA lists 12 510(k) clearances under the applicant name “Bruno Independent Living Aids, Inc.” (first 1992, latest 2012), across 5 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Bruno Independent Living Aids, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Bruno Independent Living Aids, Inc. is 26 days.

Which FDA product codes appear under Bruno Independent Living Aids, Inc.?

The most frequent FDA product codes under this applicant name are ILK (Transport, Patient, Powered, 7); ITI (Wheelchair, Powered, 2); ING (Elevator, Wheelchair, Portable, 1).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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