Company Profile
Smith+Nephew Medical Devices and Advanced Wound Care
Self-declared profile. Not yet verified by Kim Üretir. How we verify
Profile updated 1 Oct 2026Not verified yet
- Machines
- 0
- 0 verified
- Certifications
- 3
- Response time
- —
- Founded
- —
- Employees
- —
- Facility
- —
Overview
About
No English version yet — showing: —.
Language versions
- TurkishNot available
- EnglishNot available
- GermanNot available
- Simplified ChineseNot available
- Industries served
- Business languages
- Turkish
Index snapshot
How it is calculated- Machine modernity
- —/100
- Only 59 companies in the sector; no percentile shown
- Automation
- —/100
- Only 59 companies in the sector; no percentile shown
- Certification strength
- 6/100
- 85th percentile in Leather & Footwear
- Export readiness
- 0/100
- 95th percentile in Leather & Footwear
Indices are computed from profile data and are not a quality rating.
Capability matrix
Each row is a process the company performs; columns show which materials are covered and the verification level of the evidence.
No capabilities registered yet.
Machine park0 machines
No machines registered yet.
Products & HS codes
Product families the company supplies, with Harmonized System codes for customs and sourcing.
No products registered yet.
Trade & logistics
Exports
Export readiness
1/71 of 7 applicable
- Active exporter with named markets — Not declared
- Sample and series lead times — Not declared
- Minimum order value — Not declared
- Named foreign-language contact — Not declared
- Valid, verified quality certificate — Not declared
- Verified capacity report — Not declared
- Profile updated within 12 months — Met
Export readiness from published data — not a certification.
Materials
Non-Ferrous Metals
- Nitinol (NiTi Shape Memory Alloy)
Certificates
3 current · 0 expiring within 90 days · 0 expired or inactive
Product & other
ISO 10993
Biological evaluation of medical devices — biocompatibility testing (cytotoxicity, sensitization, irritation)
No expiry date- Certificate no.
- Not provided
- Issued by
- Not provided
- Accreditation
- Not provided
- Issued
- Not provided
- Valid until
- Not provided
- Scope
- Not provided
- Verification
- Unverified
FDA 510(k) / Registration
US FDA premarket notification 510(k) clearance and establishment registration / device listing (21 CFR 820 QMSR)
No expiry date- Certificate no.
- Not provided
- Issued by
- Not provided
- Accreditation
- Not provided
- Issued
- Not provided
- Valid until
- Not provided
- Scope
- Not provided
- Verification
- Unverified
FDA 21 CFR 177
US FDA food-contact compliance for polymers (indirect food additives)
No expiry date- Certificate no.
- Not provided
- Issued by
- Not provided
- Accreditation
- Not provided
- Issued
- Not provided
- Valid until
- Not provided
- Scope
- Not provided
- Verification
- Unverified
Standard codes are shown as issued and are never translated.
Quality & inspection
Quality evidence readiness
Rates the evidence published on this profile — not the quality of parts.
Quality management system0 / 25
- Best QMS certificate (tier × credit)0 / 25
Special-process approvals0 / 15
- Approvals per special-process family0 / 15
MetrologyNot applicable
Quality processes0 / 15
- First article / PPAP0 / 5
- Process capability (SPC)0 / 4
- Material traceability0 / 4
- Nonconformance handling (8D)0 / 2
Verification & freshness0 / 15
- Company verification0 / 10
- Machine verification0 / 5
Personnel qualificationNot applicable
How is this computed?
Certificate credit = validity × evidence × issuer legitimacy × completeness. Each component earns points; components that do not apply to this company are removed from the denominator. Score = 100 × points earned ÷ applicable points. A critical flag lowers the band by one level. Calibration records and company-declared quality-system details are not captured yet and count as not demonstrated.
Computed 20 Oct 2026
Quality flags
Computed automatically from the published data. A flag is a question to ask the supplier, not a verdict.
WarningNo issuing body recorded: ISO 10993, FDA 510(k) / Registration, FDA 21 CFR 177
InfoNo certificate number for a registry lookup: ISO 10993, FDA 510(k) / Registration, FDA 21 CFR 177
Quality system
- First-article inspection
- Not declared
- Process capability
- Not declared
- Traceability
- Not declared
- Non-conformance handling
- Not declared
- NDT personnel
- Not declared
- Last external audit
- Not declared
The company has not declared its quality system yet.
No quality processes registered yet.
Contact
Address
Türkiye
Website
smith-nephew.comDirect contact
Contact details as published by the company.
Company facts
- Sectors
- Leather & Footwear
- Machines
- 0 (0 verified)
- Languages
- TR
- Verification
- Unverified
Certificates
- ISO 10993 · — · Unverified
- FDA 510(k) / Registration · — · Unverified
- FDA 21 CFR 177 · — · Unverified
Contact
- Location
- Türkiye
- gbshrservices.americas@smith-nephew.com
- Web
- https://smith-nephew.com
Similar manufacturers
Ankara, Türkiye · İvedik Organised Industrial Zone
Manufacturer
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Smith+Nephew Medical Devices and Advanced Wound Care