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UNITED SURGICAL INDUSTRIES

India · Sahibabad Uttar Pradesh
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
26listed device types
Class I 22Class II 4Class III 0
plus 33 registration records and 7 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States33 registration records, 7 510(k), 0 PMA, 107 excluded
Brazil0 confirmed, 19 excluded
Saudi Arabia0 confirmed, 5 excluded
Canada0 confirmed, 9 excluded
Manufacturer names merged into this page: UNITED SURGICAL INDUSTRIES · UNITED SURGICAL LLC · UNITED SURGICAL, LTD.

Company information

Country
India
City
Sahibabad Uttar Pradesh

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

11983 · K830741
11986 · K860014
41987 · K870671
11990 · K902150

FDA listed device types

showing 8 of 26
Orthosis, Lumbar 1Splint, Hand, And Components 1Lift, Patient, Non-Ac-Powered 1Crutch 1Table, Surgical With Orthopedic Accessories, Manual 1Bed, Manual 1Orthosis, Limb Brace 1Binder, Abdominal 1

Registration details (sample)

MarketIdentifierNameClass / date
USK902150PIEZO HANDPIECE1990-07-05
USK870671PHACOTRON DAY PAK1987-04-06
USK870806NON-STERILE, EXTRA PLUS PAK CAT. #USPK 21001987-03-26

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