Alliance Medical Corp.: FDA filings under this applicant name

FDA lists 47 510(k) clearances under 2 spellings of the applicant name “Alliance Medical Corp.” (first 1994, latest 2007), across 14 product codes in 8 review panels. Median 510(k) review time under this name: 103 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
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Top product codes

Product codeDeviceSubmissions510(k) clearances
NLHCatheter, Recording, Electrode, Reprocessed1010
KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component99
JOWSleeve, Limb, Compressible88
HRXArthroscope66
GEIElectrosurgical, Cutting & Coagulation & Accessories22
IYOSystem, Imaging, Pulsed Echo, Ultrasonic22
KTWAppliance, Fixation, Nail/Blade/Plate Combination, Single Component22
NKXNeedle, Phacoemulsification, Reprocessed22
KKXDrape, Surgical, Antimicrobial11
NLMLaparoscope, General & Plastic Surgery, Reprocessed11

Plus 4 more product codes.

Review panels

Most recent Alliance Medical Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K060648REPROCESSED PHACOEMULSIFICATION TIPSNKX2007-03-19371
K061045REPROCESSED ELECTROPHYSIOLOGY CATHETERSNLH2006-08-31139
K051438VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM)JOW2006-04-04307
K060049REPROCESSED COMPRESSION SLEEVESJOW2006-02-2449
K060091ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVESJOW2006-02-1736
K053316REPROCESSED COMPRESSION SLEEVESJOW2006-02-1376
K052918REPROCESSED EXTERNAL FIXATION DEVICESKTT2006-01-27102
K052603REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERSNLH2005-11-1656
K052414REPROCESSED ELECTROPHYSIOLOGY CATHETERNLH2005-11-1675
K050518REPROCESSED PHACOEMUISIFICATION TIPSNKX2005-09-23206

37 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Alliance Medical Corp..

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.

FDA spellings included

FDA records this applicant under 2 spellings (case, punctuation and legal-suffix variants of one name); this page adds them up. Filings per spelling:

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 Alliance Medical Corp.?

FDA lists 47 510(k) clearances under 2 spellings of the applicant name “Alliance Medical Corp.” (first 1994, latest 2007), across 14 product codes in 8 review panels. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Alliance Medical Corp.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Alliance Medical Corp. is 103 days.

Which FDA product codes appear under Alliance Medical Corp.?

The most frequent FDA product codes under this applicant name are NLH (Catheter, Recording, Electrode, Reprocessed, 10); KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, 9); JOW (Sleeve, Limb, Compressible, 8).

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 (spelling variants such as punctuation and legal suffixes combined); 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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